<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href="http://www.blogger.com/styles/atom.css" type="text/css"?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:blogger='http://schemas.google.com/blogger/2008' xmlns:georss='http://www.georss.org/georss' xmlns:gd="http://schemas.google.com/g/2005" xmlns:thr='http://purl.org/syndication/thread/1.0'><id>tag:blogger.com,1999:blog-9108378134534177061</id><updated>2024-11-01T03:35:33.164-07:00</updated><category term="Class X"/><category term="Sample Paper"/><category term="Notes"/><title type='text'>Learning Fever</title><subtitle type='html'>Keep Ncert In your heart...</subtitle><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://learningfever.blogspot.com/feeds/posts/default'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/9108378134534177061/posts/default'/><link rel='alternate' type='text/html' href='http://learningfever.blogspot.com/'/><link rel='hub' href='http://pubsubhubbub.appspot.com/'/><author><name>Anonymous</name><uri>http://www.blogger.com/profile/00365631589875919657</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='https://img1.blogblog.com/img/b16-rounded.gif'/></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>3</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-9108378134534177061.post-6456229294767909728</id><published>2013-11-13T00:20:00.000-08:00</published><updated>2013-11-13T00:57:07.202-08:00</updated><category scheme="http://www.blogger.com/atom/ns#" term="Class X"/><category scheme="http://www.blogger.com/atom/ns#" term="Notes"/><title type='text'>Class 10th Carbon And Its Compound \Chemistry Notes (Ncert/Cbse)</title><content type='html'>&lt;div dir=&quot;ltr&quot; style=&quot;text-align: left;&quot; trbidi=&quot;on&quot;&gt;
&lt;div style=&quot;font-family: segoe ui;&quot;&gt;
&lt;div dir=&quot;ltr&quot; style=&quot;text-align: left;&quot; trbidi=&quot;on&quot;&gt;
&lt;h2 style=&quot;color: #006666; font-size: medium;&quot;&gt;
Carbon and Its Compounds&lt;/h2&gt;
&lt;h3 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
Carbon: Introduction&lt;/h3&gt;
Atomic Number: 6&lt;br /&gt;
Electronic Configuration: 2, 4.&lt;br /&gt;
Valence electrons: 4&lt;br /&gt;
Property: Non-metal&lt;br /&gt;
Abundance:- Carbon is the 4th most abundant substance in universe and 15th most 
    abundant substance in the earth’s crust. &lt;br /&gt;
Compounds having carbon atoms among the components are known as carbon compounds. 
    Previously, carbon compounds could only be obtained from a living source; hence 
    they are also known as organic compounds. &lt;br /&gt;
&lt;h4 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;
    Bonding In Carbon:- The Covalent Bond&lt;/span&gt;&lt;/h4&gt;
Bond formed by sharing of electrons is called covalent bond. Two of more atoms 
    share electrons to make their configuration stable. In this type of bond, all 
    the atoms have similar rights over shared electrons. Compounds which are formed 
    because of covalent bond are called COVALNET COMPOUNDS. &lt;br /&gt;
Covalent bonds are of three types: Single, double and triple covalent bond. &lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Single Covalent Bond:&lt;/span&gt; Single covalent bond is 
    formed because of sharing of two electrons, one from each of the two atoms. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of hydrogen molecule (H&lt;sub&gt;2&lt;/sub&gt;) &lt;/div&gt;
Atomic Number of H = 1&lt;br /&gt;
Electronic configuration of H = 1.&lt;br /&gt;
Valence electron of H = 1&lt;br /&gt;
Hydrogen forms duet, to obtain stable configuration. This configuration is 
    similar to helium (a noble gas). &lt;br /&gt;
Since, hydrogen has one electron in its valence shell, so it requires one more 
    electron to form a duet. So, in the formation of hydrogen molecule; one electron 
    from each of the hydrogen atoms is shared. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image1&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon1.PNG&quot; style=&quot;border-width: 0px; height: 72px; width: 352px;&quot; /&gt;
    
&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of hydrogen chloride (HCl): &lt;/div&gt;
Valence electron of hydrogen = 1&lt;br /&gt;
Atomic number of chlorine = 17&lt;br /&gt;
Electronic configuration of chlorine: 2, 8, 7&lt;br /&gt;
Electrons in outermost orbit = 7&lt;br /&gt;
Valence electron = 7&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image2&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon2.PNG&quot; style=&quot;border-width: 0px; height: 44px; width: 350px;&quot; /&gt;
    
 &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of chlorine molecule (Cl&lt;sub&gt;2&lt;/sub&gt;): &lt;/div&gt;
Valence electron of chlorine = 7&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image3&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon3.PNG&quot; style=&quot;border-width: 0px; height: 63px; width: 350px;&quot; /&gt;
&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of water (H&lt;sub&gt;2&lt;/sub&gt;O) &lt;/div&gt;
Valence electron of hydrogen = 1&lt;br /&gt;
Atomic number of oxygen = 8&lt;br /&gt;
Electronic configuration of oxygen = 2, 6&lt;br /&gt;
Valence electron = 6&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image4&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon4.PNG&quot; style=&quot;border-width: 0px; height: 38px; width: 351px;&quot; /&gt;
    
Oxygen in water molecule completes stable configuration by the sharing one 
    electron from each of the two hydrogen atoms. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Methane (CH&lt;sub&gt;4&lt;/sub&gt;) &lt;/div&gt;
Valence electron of carbon = 4&lt;br /&gt;
Valence electron of hydrogen = 1&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image5&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon5.PNG&quot; style=&quot;border-width: 0px; height: 82px; width: 356px;&quot; /&gt;
&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Ethane (C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;6&lt;/sub&gt;): &lt;/div&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image6&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon6.PNG&quot; style=&quot;border-width: 0px; height: 52px; width: 350px;&quot; /&gt;
    
 &lt;br /&gt;
&lt;h5 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;
     &lt;span style=&quot;color: #0066cc;&quot;&gt;Double covalent bond:&lt;/span&gt; Double bond is formed 
     by sharing of four electrons, two from each of the two atoms.
     &lt;/span&gt; &lt;/h5&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of oxygen molecule (O&lt;sub&gt;2&lt;/sub&gt;): &lt;/div&gt;
Valence electron of oxygen = 2&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image7&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon7.PNG&quot; style=&quot;border-width: 0px; height: 39px; width: 350px;&quot; /&gt;
    
 In the formation of oxygen molecule, two electrons are shared by each of the two 
     oxygen atoms to complete their stable configuration. &lt;br /&gt;
In oxygen, the total number of shared electrons is four, two from each of the 
    oxygen atoms. So a double covalent bond is formed. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Carbon dioxide (CO&lt;sub&gt;2&lt;/sub&gt;): &lt;/div&gt;
Valence electron of carbon = 4&lt;br /&gt;
Valence electron of oxygen = 6&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image8&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon8.PNG&quot; style=&quot;border-width: 0px; height: 22px; width: 350px;&quot; /&gt;
In carbon dioxide two double covalent bonds are formed. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Ethylene (C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;): &lt;/div&gt;
Valence electron of carbon = 4&lt;br /&gt;
Valence electron of hydrogen = 1&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image9&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon9.PNG&quot; style=&quot;border-width: 0px; height: 55px; width: 351px;&quot; /&gt;
Triple Covalent Bond: Triple covalent bond is formed because of the sharing of 
    six electrons, three from each of the two atoms. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Nitrogen (N&lt;sub&gt;2&lt;/sub&gt;): &lt;/div&gt;
Atomic number of nitrogen = 7&lt;br /&gt;
Electronic configuration of nitrogen = 2, 5&lt;br /&gt;
Valence electron = 5&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image10&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon10.PNG&quot; style=&quot;border-width: 0px; height: 87px; width: 402px;&quot; /&gt;
  In the formation of nitrogen, three electrons are shared by each of the nitrogen 
      atoms. Thus one triple bond is formed because of the sharing of total six 
      electrons. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Formation of Acetylene (C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;2&lt;/sub&gt;): &lt;/div&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image11&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon11.PNG&quot; style=&quot;border-width: 0px; height: 64px; width: 381px;&quot; /&gt;
    
&lt;br /&gt;
&lt;h6 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
Properties of Covalent Bond: &lt;/h6&gt;
&lt;ul&gt;
&lt;li&gt;Intermolecular force is smaller. &lt;/li&gt;
&lt;li&gt;Covalent bonds are weaker than ionic bond. As a result, covalent compounds have 
                low melting and boiling points. 
            &lt;/li&gt;
&lt;li&gt;Covalent compounds are poor conductor of electricity as no charged particles are 
                formed in covalent bond. 
            &lt;/li&gt;
&lt;li&gt;Since, carbon compounds are formed by the formation of covalent bond, so carbon 
                compounds generally have low melting and boiling points and are poor conductor 
                of electricity. 
            &lt;/li&gt;
&lt;/ul&gt;
&lt;br /&gt;
Organic Compounds: &lt;br /&gt;
Initially, compounds of carbon could only be obtained from living sources and 
    there was no way of synthesizing them. Hence, carbon compounds are also known as 
    organic compounds. &lt;br /&gt;
Carbon forms a large number of compounds. So far, formulae of about 3 million 
    carbon compounds are known. &lt;br /&gt;
Cause of formation of such a large number of compounds by carbon:- &lt;br /&gt;
(a) Carbon can form bonds with other carbon atoms. This property of carbon is 
    known as CATENATION. Because of catenation, carbon can form a long chain; while 
    making bond with other carbon atoms. Carbon can make single, double and triple 
    bonds by catenation. &lt;br /&gt;
Example: &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image1&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon12.PNG&quot; style=&quot;border-width: 0px; height: 123px; width: 450px;&quot; /&gt; 
             
            
 (c) Carbon can form branched chain; along with straight chain; while combining 
    with carbon atoms, i.e. because of the property of catenation. &lt;br /&gt;
Example:- &lt;br /&gt;
(b) Carbon has four electrons in its outermost orbit. This gives carbon the 
    valency which is equal to 4. That’s why carbon is tetravalent. &lt;br /&gt;
Carbon can also form bonds with other types of monovalent atoms; apart from 
    carbon. Carbon can make long chain combining with other atoms also. For example; 
    carbon can form bonds with oxygen, hydrogen, nitrogen, etc. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image2&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon13.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;
Carbon-carbon bonds are very stable, which makes the compounds of carbon 
    stable. &lt;br /&gt;
Hydrocarbon: &lt;br /&gt;
Hydrogen + Carbon = Hydrocarbon.&lt;br /&gt;
Compounds; formed because of the combination of 
        hydrogen and carbon are known as hydrocarbons. &lt;br /&gt;
Types of hydrocarbon: Saturated and Unsaturated. &lt;br /&gt;
Saturated hydrocarbons: &lt;br /&gt;
Hydrocarbons having single bonds are known as SATURATED HYDROCARBONS. Saturated 
    hydrocarbons are known as ALKANE. These are also known as paraffin. &lt;br /&gt;
Example: Methane, Ethane, Propane, etc. &lt;br /&gt;
Unsaturated hydrocarbon: Unsaturated hydrocarbons are of two types – Hydrocarbon 
        with double bond and hydrocarbon with triple bond. &lt;br /&gt;
Hydrocarbon with double bond: Hydrocarbons having at least one double bond are 
    known as ALKENE&lt;br /&gt;
Example:- &lt;br /&gt;
Ethylene, Propylene, Butylene, etc. &lt;br /&gt;
Hydrocarbon with triple bond: Hydrocarbons having at least one triple bond are 
    known as ALKYNE. &lt;br /&gt;
Example: &lt;br /&gt;
Ethyne, Propyne, Butyne, etc. &lt;br /&gt;
ALKANE: Hydrocarbons having only single bonds are known as alkane. These are 
    saturated hydrocarbons. Alkane are also known as paraffin. &lt;br /&gt;
&lt;b&gt;(a)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image3&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon14.PNG&quot; style=&quot;border-width: 0px; height: 133px; width: 272px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(b)&lt;/b&gt;&lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image4&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon15.PNG&quot; style=&quot;border-width: 0px; height: 170px; width: 556px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(c)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image5&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon16.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(d)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image6&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon17.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(e)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image7&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon18.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(f)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image8&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon19.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(g)&lt;/b&gt;&lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image9&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon20.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt; (h)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image10&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon21.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(i)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image11&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon22.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;b&gt;(j)&lt;/b&gt; &lt;img align=&quot;texttop&quot; id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image12&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon23.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image13&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon24.PNG&quot; style=&quot;border-width: 0px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;h3 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
Carbon: Unsaturated 
        Hydrocarbons: Alkene and Alkyne&lt;/h3&gt;
&lt;h4 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;color: #0066cc; font-weight: normal;&quot;&gt;ALKENE:-&lt;/span&gt;&lt;span style=&quot;font-weight: normal;&quot;&gt; Hydrocarbons having at least one double bond between two carbon atoms are known as ALKENE.
    &lt;/span&gt; &lt;/h4&gt;
Alkane – ane + ene = Alkene.&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image1&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon25.PNG&quot; style=&quot;border-width: 0px; height: 49px; width: 248px;&quot; /&gt; 
Name of this compound: Since, hydrocarbon having one carbon atom is known as Methane. &lt;br /&gt;
Thus, Methane – ane + ene = Methene&lt;br /&gt;
But, alkene does not exist with one carbon atom, thus, methene does not exist. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image2&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon26.PNG&quot; style=&quot;border-width: 0px; height: 279px; width: 234px;&quot; /&gt;  
In similar way, other Alkenes are formed. &lt;br /&gt;
&lt;h5 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;color: #0066cc; font-weight: normal;&quot;&gt;ALKYNE:&lt;/span&gt;&lt;span style=&quot;font-weight: normal;&quot;&gt; Hydrocarbons having at least one triple bond between two carbon atoms are known as alkyne.
    &lt;/span&gt; &lt;/h5&gt;
Alkane – ane + yne = Alkyne&lt;br /&gt;
Similarly, &lt;br /&gt;
Ethane – ane + yne = Ethyne &lt;br /&gt;
Propane – ane + yne = Propyne &lt;br /&gt;
Butane – ane + yne = Butyne&lt;br /&gt;
Pentane – ane + yne = Pentyne&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image3&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon27.PNG&quot; style=&quot;border-width: 0px; height: 438px; width: 329px;&quot; /&gt;  

In similar way other Alkynes are formed. &lt;br /&gt;
&lt;h6 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Cyclic Hydrocarbon:- 
    &lt;/span&gt; &lt;/h6&gt;
Carbon can form cyclic structure combining with carbon atoms. Such hydrocarbons are known as cyclic hydrocarbon. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image4&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon28.PNG&quot; style=&quot;border-width: 0px; height: 301px; width: 402px;&quot; /&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;h3 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
Carbon: Functional Group And Nomenclature of Hydrocarbon&lt;/h3&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Functional Group: &lt;/div&gt;
&lt;h4 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Single 
atom or group of atoms, that have similar chemical properties are called
 functional group. For example: Halogen group, Carboxyl group, Aldehyde 
group, etc. 
    &lt;/span&gt; &lt;/h4&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Alkyl group:&lt;/span&gt; -R is known as alkyl group. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image1&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon29.PNG&quot; style=&quot;border-width: 0px; height: 116px; width: 400px;&quot; /&gt;&lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Halogen group:&lt;/span&gt; Halogen group is also known as halo group. –Cl (Chloro),-Br(Bromo),-I(Iodo) are halogen or halo group. &lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Alcohol:&lt;/span&gt; -OH is known as alcohol group.&lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Aldehyde:&lt;/span&gt; -CHO is known as aldehyde group. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image2&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon30.PNG&quot; style=&quot;border-width: 0px; height: 213px; width: 500px;&quot; /&gt;
&lt;br /&gt;
Hydrocarbons belong to same group have similar properties. &lt;br /&gt;
&lt;h5 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Nomenclature of Carbon Compounds: 
    &lt;/span&gt; &lt;/h5&gt;
International Union of 
Pure and Applied Chemistry (IUPAC) decided some rules to name the carbon
 compounds. This was done to maintain the uniformity throughout the 
world. Names which are given on this basis are popularly known as IUPAC 
name. &lt;br /&gt;
(1) Identify the number of carbon atoms in carbon compound. Name the carbon compounds according to the number of carbon atoms. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Example:- &lt;/div&gt;
Saturated hydrocarbon having one carbon atom is named as Methane. 
Saturated hydrocarbon having two carbon atoms is named as Ethane. &lt;br /&gt;
Unsaturated hydrocarbon with double bond having two carbon atoms is named as Ethene. &lt;br /&gt;
Unsaturated hydrocarbon with triple bond between carbon atoms is named as Ethyne. &lt;br /&gt;
(2) If the structure has branched chain, identify the longest chain and then identify the number of carbon atoms. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image3&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon31.PNG&quot; style=&quot;border-width: 0px; height: 142px; width: 484px;&quot; /&gt;&lt;br /&gt;
In figure (a) the longest chain has eight carbon atoms, and thus the 
name of parent compound would be octane. In figure (b) longest chain has
 nine carbon atoms, and thus the name of parent compound would be 
nonane.&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image4&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon32.PNG&quot; style=&quot;border-width: 0px; height: 100px; width: 300px;&quot; /&gt;&lt;br /&gt;
Identify the longest chain. Then number the carbon atoms in such a 
fashion that the functional group; if any; would come at the lowest 
number. &lt;br /&gt;
In the given figure (c), while counting from right to left (in red 
color), branched chain which is functional group falls at the fourth 
position. On the other hand, while counting from left to right, the 
branched chain falls at the fifth position. In this case, the numbering 
from right to left is taken because then only the functional would be at
 the lowest position. &lt;br /&gt;
(3) In case of a functional group present, write the prefix or 
suffix of the functional group according to the table given here. Then 
write the name of the parent compound. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image5&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon33.PNG&quot; style=&quot;border-width: 0px; height: 227px; width: 330px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Nomenclature of Alkane:- &lt;/div&gt;
Example – (1) &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image6&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon34.PNG&quot; style=&quot;border-width: 0px; height: 215px; width: 504px;&quot; /&gt;
&lt;br /&gt;
Common name:- Iso-butane. &lt;br /&gt;
IUPAC Name: &lt;br /&gt;
Number of carbon atoms in the longest chain = 3. &lt;br /&gt;
A methyl group is present at carbon number 2. &lt;br /&gt;
So, IUPAC Name is 2-methyl propane. &lt;br /&gt;
Example:- (2) -&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image7&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon35.PNG&quot; style=&quot;border-width: 0px; height: 193px; width: 399px;&quot; /&gt;&lt;br /&gt;
It’s common name is Iso-pentane. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
IUPAC Name: &lt;/div&gt;
Numbering of carbon atoms is done in two ways, i.e. from left to right and from right to left. &lt;br /&gt;
The number of carbon atoms in the longest chain = 4. &lt;br /&gt;
A methyl group (functional group) is attached with this chain. &lt;br /&gt;
Thus, name of parent compound is Butane. &lt;br /&gt;
In the numbering from left to right functional group falls at second 
number while in the numbering from right to left; the functional group 
falls at 3rd position. &lt;br /&gt;
Therefore, IUPAC name of this compound is 2-methyl butane. &lt;br /&gt;
Example:(3):-&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image8&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon36.PNG&quot; style=&quot;border-width: 0px; height: 150px; width: 110px;&quot; /&gt;&lt;br /&gt;
Common name: NeopentaneAC Name: There are three carbon atoms in longest chain. &lt;br /&gt;
Two methyl groups are present at second (2) carbon atom. (Di is used as prefix for two). &lt;br /&gt;
Therefore, IUPAC Name: Di-methyl propane. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Naming of hydrocarbon with Halo group: &lt;/div&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image9&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon37.PNG&quot; style=&quot;border-width: 0px; height: 64px; width: 115px;&quot; /&gt;&lt;br /&gt;
Common name: Methyl chloride&lt;br /&gt;
There is one carbon atom in this compound. So its parent name is Methane. &lt;br /&gt;
One chloro group is present in this compound. &lt;br /&gt;
So, its IUPAC name is Chloro-methane. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image10&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon38.PNG&quot; style=&quot;border-width: 0px; height: 65px; width: 113px;&quot; /&gt;&lt;br /&gt;
Common Name: Propyl chloride. AC Name: &lt;br /&gt;
Number of carbon atoms = 3&lt;br /&gt;
Functional group: Chloro&lt;br /&gt;
Thus, IUPAC Name is Chloro-propane. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image11&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon39.PNG&quot; style=&quot;border-width: 0px; height: 60px; width: 133px;&quot; /&gt;&lt;br /&gt;
Common name: Propyl brominde&lt;br /&gt;
IUPAC Name: Bromo-propane&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image12&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon40.PNG&quot; style=&quot;border-width: 0px; height: 65px; width: 117px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 6 (six) ctional group: Iodo&lt;br /&gt;
Common Name: Hexyl iodide. &lt;br /&gt;
IUPAC Name: Iodo-hexane. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image13&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon41.PNG&quot; style=&quot;border-width: 0px; height: 82px; width: 188px;&quot; /&gt;&lt;br /&gt;
Number of carbon atom: 1 (one) &lt;br /&gt;
Functional group: Alcohol (suffix : ol) &lt;br /&gt;
Common name: Methyl alcohol. &lt;br /&gt;
IUPAC Name: &lt;br /&gt;
Methane – e Methane – e + ol = Methanol. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image14&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon42.PNG&quot; style=&quot;border-width: 0px; height: 69px; width: 149px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 2 (two) &lt;br /&gt;
Functional group: Alcohol&lt;br /&gt;
Common name: Ethyl alcohol. &lt;br /&gt;
IUPAC Name: EthanoIUPAC Name: Ethanol. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image15&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon43.PNG&quot; style=&quot;border-width: 0px; height: 75px; width: 153px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 6 (six) l group: Alcohol&lt;br /&gt;
Common name: Hexyl alcohol. &lt;br /&gt;
IUPAC IUPAC Name: Hexanol. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Naming of Aldehyde group (-CHO): &lt;/div&gt;
The suffix of aldehyde group is “al”. &lt;br /&gt;
IUPAC name of alkane having aldehyde group is written as follows: &lt;br /&gt;
Alkane – e + al = Alkanal&lt;br /&gt;
Methane – e + al = Methanal&lt;br /&gt;
Ethane – e + al = Ethanal, and so on. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image16&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon44.PNG&quot; style=&quot;border-width: 0px; height: 66px; width: 139px;&quot; /&gt;&lt;br /&gt;
Number of carbon atom: 1 (one)  &lt;br /&gt;
IUPAC Name: Methanal&lt;br /&gt;
Common name: Formaldehyde. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image17&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon45.PNG&quot; style=&quot;border-width: 0px; height: 67px; width: 150px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 2 (Two) &lt;br /&gt;
Functional group: Aldehyde &lt;br /&gt;
IUPAC Name: Ethanal&lt;br /&gt;
Common name: Acetaldehyde&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image18&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon46.PNG&quot; style=&quot;border-width: 0px; height: 67px; width: 152px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 7 (seven) C Number of carbon atoms: 7 (seven) C Name: Heptanal. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Naming of Carboxylic Acid (– COOH): &lt;/div&gt;
Suffix for carboxylic acid is ‘oic acid”. &lt;br /&gt;
Thus an alkane having carboxylic acid is named as: &amp;gt;Example: &lt;br /&gt;
Methane – e + oic acid = Methanoic acid&lt;br /&gt;
Ethane – e + oic acid = Ethanoic acid. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image19&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon47.PNG&quot; style=&quot;border-width: 0px; height: 48px; width: 218px;&quot; /&gt;
&lt;br /&gt;
Number of carbon atom: 1(one)&lt;br /&gt;
IUPAC Name: Methanoic acid. &lt;br /&gt;
Common name: Formic acid. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image20&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon48.PNG&quot; style=&quot;border-width: 0px; height: 77px; width: 159px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 2 (two) &lt;br /&gt;
Common Name: Acetic acid. &lt;br /&gt;
IUPAC Name: Ethanoic Acid&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image21&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon49.PNG&quot; style=&quot;border-width: 0px; height: 69px; width: 156px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 5 (five) &lt;br /&gt;
Functional group present: Carboxylic acid&lt;br /&gt;
IUPAC Name: Pentanoic acid. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Naming of Ketone (– CO –):&lt;/div&gt;
Suffix for ketone group: ‘one’. &lt;br /&gt;
A hydrocarbon having ketone group is named as: &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image22&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon50.PNG&quot; style=&quot;border-width: 0px; height: 106px; width: 179px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 3 (three) &lt;br /&gt;
Functional group: Ketone group&lt;br /&gt;
Thus, IUPAC Name is Propanone. &lt;br /&gt;
Common name: Dimethyl ketone. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image23&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon51.PNG&quot; style=&quot;border-width: 0px; height: 121px; width: 263px;&quot; /&gt;&lt;br /&gt;
Number of carbon atoms: 5 (five) &lt;br /&gt;
Functional group: Ketone group&lt;br /&gt;
Thus, IUPAC Name: Pentanone&lt;br /&gt;
General name: Diethyl ketone&lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image24&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon52.PNG&quot; style=&quot;border-width: 0px; height: 107px; width: 179px;&quot; /&gt;
&lt;br /&gt;
Number of carbon atoms: 6 (six) &lt;br /&gt;
IUPAC Name: Hexanone&lt;br /&gt;
General name: Ethyl propyl ketone&lt;br /&gt;
&lt;h6 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Homologous Series: 
    &lt;/span&gt; &lt;/h6&gt;
Series of compounds with same general formula and functional group is
 known as homologous series. Compounds belonging to the same homologous 
series show similar properties. Compounds of homologous series differ by
 CH&lt;sub&gt;2&lt;/sub&gt; from their consecutive members. Each subsequent compound in a homologous series differs by 14 au. &lt;br /&gt;
Example: &lt;br /&gt;
Alkanes, such as, Methane, Ethane, Propane, Butane, etc. belong to same homologous series. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image25&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon53.PNG&quot; style=&quot;border-width: 0px; height: 39px; width: 364px;&quot; /&gt;&lt;br /&gt;
Similarly, all alkenes and alkSimilarly, all alkenes and alkynes belong to same homologous series. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Properties of Compounds of Same Homologous Series&lt;/div&gt;
(a) Compounds of same homologous series have same general formula. &lt;br /&gt;
(b) Compounds of same homologous series differ from their 
consecutive members by one carbon atom and two hydrogen atoms, 
homologous series differ from their consecutive members by 
    one carbon atom and two hydrogen atoms, i.e. by CH&lt;sub&gt;2&lt;/sub&gt;&lt;br /&gt;
(d) Compounds of same homologous series have same chemical properties. &lt;br /&gt;
(e)Compounds of same homologous series differ by physical properties with increase or decrease in molecular mass.&lt;br /&gt;
&lt;br /&gt;
&lt;h3 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
Carbon: Chemical Properties of Carbon Compounds&lt;/h3&gt;
&lt;h4 style=&quot;color: #0066cc; font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Combustion or Combustion Reaction: 
    &lt;/span&gt; &lt;/h4&gt;
&lt;h5 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Carbon and carbon compounds gives carbon dioxide, vapor, heat and light on burning in air. 
    &lt;/span&gt; &lt;/h5&gt;
Example: &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image1&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon54.PNG&quot; style=&quot;border-width: 0px; height: 109px; width: 466px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Oxidation: &lt;/div&gt;
In combustion reaction, carbon compounds are oxidized in the presence
 of oxygen. The following example is different because alkaline KMnO&lt;sub&gt;4&lt;/sub&gt; is the oxidizing agent in this reaction. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image2&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon55.PNG&quot; style=&quot;border-width: 0px; height: 44px; width: 475px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Addition Reaction:- &lt;/div&gt;
&lt;h6 style=&quot;font-size: small;&quot;&gt;
&lt;span style=&quot;font-weight: normal;&quot;&gt;Formation of larger molecules by addition of more radicals is known as addition reaction. 
    &lt;/span&gt; &lt;/h6&gt;
Ethene is converted into ethane when heated with the catalyst nickel. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image3&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon56.PNG&quot; style=&quot;border-width: 0px; height: 121px; width: 427px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Substitution Reaction: &lt;/div&gt;
Replacement of a functional group or any atom by another atom or 
functional group is known as substitution reaction. Substitution 
reactions are single displacement reactions. &lt;br /&gt;
When methane reacts with chlorine gas in the presence of sunlight, it gives chloromethane and hydrogen chloride. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image4&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon57.PNG&quot; style=&quot;border-width: 0px; height: 156px; width: 439px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Some Important Carbon Compounds: Ethanol and Ethanoic Acid: &lt;/div&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
&lt;b&gt;Ethanol (C&lt;sub&gt;2&lt;/sub&gt;&lt;/b&gt;H&lt;b&gt;&lt;sub&gt;5&lt;/sub&gt;OH): &lt;/b&gt; &lt;/div&gt;
&lt;ul&gt;
&lt;li&gt;Ethanol is commonly known as alcohol and spirit. &lt;/li&gt;
&lt;li&gt;General name of ethanol is ethyl alcohol. &lt;/li&gt;
&lt;li&gt;Ethanol is the main constituent of all alcoholic drinks &lt;/li&gt;
&lt;li&gt;Ethanol is soluble in water &lt;/li&gt;
&lt;li&gt;Ethanol is a very good solvent &lt;/li&gt;
&lt;li&gt;Ethanol is used in manufacturing of medicines, such as tincture iodine, cough syrup, etc. 
        &lt;/li&gt;
&lt;li&gt;Taking even small quantity of pure ethanol may prove lethal &lt;/li&gt;
&lt;li&gt;Taking dilute ethyl alcohol can cause drunkenness &lt;/li&gt;
&lt;li&gt;Reaction of ethanol with sodium metal: &lt;/li&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image5&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon58.PNG&quot; style=&quot;border-width: 0px; height: 294px; width: 461px;&quot; /&gt;&lt;br /&gt;
&lt;li&gt;General name of ethanoic acid is acetic acid. &lt;/li&gt;
&lt;li&gt;Melting point of ethanoic acid is 290K. &lt;/li&gt;
&lt;li&gt;Ethanoic acid freezes in winter and hence it is also known as glacial acetic acid. 
        &lt;/li&gt;
&lt;li&gt;Ethanoic acid is a colorless liquid. &lt;/li&gt;
&lt;li&gt;5% to 8% solution of acetic acid in water is known as vinegar. &lt;/li&gt;
&lt;li&gt;Vinegar is used as preservative in pickles. &lt;/li&gt;
&lt;li&gt;Carboxylic acids are weak acid compared to mineral acids. &lt;/li&gt;
&lt;/ul&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Reaction of ethanoic acid with base: &lt;/div&gt;
Ethanoic acid gives sodium acetate when it reacts with sodium hydroxide. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image6&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon59.PNG&quot; style=&quot;border-width: 0px; height: 171px; width: 433px;&quot; /&gt;&lt;br /&gt;
The IUPAC name of Ethyl acetate is Ethyl Ethanoate. Ethyl acetate is also known as ester. &lt;br /&gt;
Ester is a sweet smelling compound. It is used in making perfumes and as a flavouring agent. &lt;br /&gt;
When ethyl ethanoate reacts with a base or acid, it gives back ethanol and ethanoic acid. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image7&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon60.PNG&quot; style=&quot;border-width: 0px; height: 68px; width: 387px;&quot; /&gt;&lt;br /&gt;
This reaction is called saponification, since it is used in making of soap. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Hydrolysis of ester (Ethyl ethanoate): &lt;/div&gt;
Ethyl ethanoate gives parent alcohol and sodium ethanoate when heated with sodium hydroxide solution. &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image8&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon61.PNG&quot; style=&quot;border-width: 0px; height: 78px; width: 408px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Saponification: &lt;/div&gt;
Ester of higher fatty acids gives sodium salt of higher fatty acid; 
when heated with glycerol and sodium hydroxide. Sodium salts of higher 
fatty acid are known as soaps. This reaction is called saponification 
(soap making). &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Reaction of ethanoic acid with sodium carbonate and sodium bicarbonate: &lt;/div&gt;
Ethanoic acid gives sodium acetate, water and carbon dioxide when 
reacts with sodium carbonate or sodium bicarbonate (sodium hydrogen 
carbonate). &lt;br /&gt;
&lt;img id=&quot;ctl00_ctl00_ContentPlaceHolder1_ContentPlaceHolder3_Image9&quot; src=&quot;http://www.excellup.com/classten/scienceten/ImageCarbon/Carbon62.PNG&quot; style=&quot;border-width: 0px; height: 66px; width: 413px;&quot; /&gt;&lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Soaps and Detergents: &lt;/div&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Soap:&lt;/span&gt; Ester of higher fatty acids
 is called soap. It is manufactured by the reaction of easter of higher 
fatty acid with sodium hydroxide. The sodium salt so formed has 
cleansing property. &lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Detergent:&lt;/span&gt; Soap cannot form 
lather in hard water. To overcome this problem, detergents were 
introduced. Detergent is also known as soapless soap. &lt;br /&gt;
Detergent is sodium salt of benzene sulphonic acid or sodium salt of long chain alkyl hydrogen sulphate. &lt;br /&gt;
&lt;div style=&quot;color: #0066cc;&quot;&gt;
Cleansing action of soap: &lt;/div&gt;
Soap molecule has two ends. One end is hydrophilic and another end is
 hydrophobic. In other words, one end is lipophobic (hydrophilic) and 
another end is lipophilic (hydrophobic). When soap is dissolved in water
 and clothes are put in the soapy solution, soap molecules converge in a
 typical fashion to make a structure; called micelle. The hydrophobic 
ends of different molecules surround a particle of grease and make the 
micelle; which is a spherical structure. In this, the hydrophilic end is
 outside the sphere and hydrophobic end is towards the centre of the 
sphere. That is how, soap molecules wash away dirt and grease by making 
micelles around them.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;span style=&quot;color: #0066cc;&quot;&gt;Soap and Hard Water:&lt;/span&gt; Hard water 
often contains salts of calcium and magnesium. Soap molecules react with
 the salts of calcium and magnesium and form a precipitate. This 
precipitate begins floating as an off-white layer over water. This layer
 is called scum. Soaps lose their cleansing property in hard water 
because of formation of scum. Detergents are used; instead of soaps; in 
hard water to overcome the problem. Detergents are usually ammonium or 
sulphonate salts of carboxylic acids. The charged ends of these 
compounds do not form precipitate with calcium or magnesium salts in 
hard water. Hence, detergents retain their cleansing property in hard 
water. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&amp;nbsp;Download Notes From Given Link Below:&lt;/span&gt;&lt;br /&gt;
&lt;a href=&quot;http://www.uploadmb.com/dw.php?id=1384330472&quot; target=&quot;_blank&quot;&gt;&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&lt;br /&gt;&lt;/span&gt;&lt;/a&gt;
&lt;a href=&quot;http://www.uploadmb.com/dw.php?id=1384330472&quot; target=&quot;_blank&quot;&gt;&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;Download Notes Now&lt;/span&gt;&lt;/a&gt;&lt;/div&gt;
&lt;div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
</content><link rel='replies' type='application/atom+xml' href='http://learningfever.blogspot.com/feeds/6456229294767909728/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://learningfever.blogspot.com/2013/11/class-10th-carbon-and-its-compound.html#comment-form' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/9108378134534177061/posts/default/6456229294767909728'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/9108378134534177061/posts/default/6456229294767909728'/><link rel='alternate' type='text/html' href='http://learningfever.blogspot.com/2013/11/class-10th-carbon-and-its-compound.html' title='Class 10th Carbon And Its Compound \Chemistry Notes (Ncert/Cbse)'/><author><name>Anonymous</name><uri>http://www.blogger.com/profile/00365631589875919657</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='https://img1.blogblog.com/img/b16-rounded.gif'/></author><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-9108378134534177061.post-8460518245467962909</id><published>2013-11-12T23:48:00.001-08:00</published><updated>2013-11-13T00:27:33.912-08:00</updated><category scheme="http://www.blogger.com/atom/ns#" term="Class X"/><category scheme="http://www.blogger.com/atom/ns#" term="Sample Paper"/><title type='text'>Science SA-II Sample Paper | Class 10</title><content type='html'>&lt;div dir=&quot;ltr&quot; style=&quot;text-align: left;&quot; trbidi=&quot;on&quot;&gt;
&lt;span style=&quot;font-size: large;&quot;&gt;&lt;a href=&quot;https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhzF-3Ch0jkAcDRv_Koxlfo_wg4eSYo4B7tsHSFcleHNwbdSmMBx15_aw-KfLroHoEgKW5PzVvN5sew_l-Zj6kFr-nbHnwnND5QBDIVxkysXIGOMvwRsyO2suR-WUDtcspfRSxl57cLRCs/s1600/science.png&quot; imageanchor=&quot;1&quot; style=&quot;clear: left; float: left; margin-bottom: 1em; margin-right: 1em;&quot;&gt;&lt;img border=&quot;0&quot; height=&quot;320&quot; src=&quot;https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhzF-3Ch0jkAcDRv_Koxlfo_wg4eSYo4B7tsHSFcleHNwbdSmMBx15_aw-KfLroHoEgKW5PzVvN5sew_l-Zj6kFr-nbHnwnND5QBDIVxkysXIGOMvwRsyO2suR-WUDtcspfRSxl57cLRCs/s320/science.png&quot; width=&quot;320&quot; /&gt;&lt;/a&gt;&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;Download Science SA-II Sample Paper Class 10 from given link below:&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&lt;br /&gt;&lt;/span&gt;
&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&lt;span style=&quot;font-size: large;&quot;&gt;&lt;a href=&quot;http://www.cbse.nic.in/curric~1/sqp_term1_sep11/SQP_SC_X_I.pdf&quot; target=&quot;_blank&quot;&gt;Download/view&lt;/a&gt;&lt;/span&gt;&lt;/span&gt;&lt;br /&gt;
&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&lt;br /&gt;&lt;/span&gt;
&lt;br /&gt;
&lt;br /&gt;&lt;span style=&quot;font-family: Georgia,&amp;quot;Times New Roman&amp;quot;,serif;&quot;&gt;&lt;span style=&quot;color: red;&quot;&gt;Note: If you won&#39;t able to download it sample paper then simply right click on &quot;View/Download&quot; and click &lt;b&gt;Save as &lt;/b&gt;or&lt;b&gt; Save target as&quot;&lt;/b&gt;&lt;/span&gt;&lt;/span&gt;
&lt;/div&gt;
</content><link rel='replies' type='application/atom+xml' href='http://learningfever.blogspot.com/feeds/8460518245467962909/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='http://learningfever.blogspot.com/2013/11/science-sa-ii-sample-paper-class-10.html#comment-form' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/9108378134534177061/posts/default/8460518245467962909'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/9108378134534177061/posts/default/8460518245467962909'/><link rel='alternate' type='text/html' href='http://learningfever.blogspot.com/2013/11/science-sa-ii-sample-paper-class-10.html' title='Science SA-II Sample Paper | Class 10'/><author><name>Anonymous</name><uri>http://www.blogger.com/profile/00365631589875919657</uri><email>noreply@blogger.com</email><gd:image rel='http://schemas.google.com/g/2005#thumbnail' width='16' height='16' src='https://img1.blogblog.com/img/b16-rounded.gif'/></author><media:thumbnail xmlns:media="http://search.yahoo.com/mrss/" url="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhzF-3Ch0jkAcDRv_Koxlfo_wg4eSYo4B7tsHSFcleHNwbdSmMBx15_aw-KfLroHoEgKW5PzVvN5sew_l-Zj6kFr-nbHnwnND5QBDIVxkysXIGOMvwRsyO2suR-WUDtcspfRSxl57cLRCs/s72-c/science.png" height="72" width="72"/><thr:total>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-9108378134534177061.post-6097564576096817542</id><published>2013-11-08T21:51:00.001-08:00</published><updated>2014-03-16T12:17:18.278-07:00</updated><category scheme="http://www.blogger.com/atom/ns#" term="Class X"/><category scheme="http://www.blogger.com/atom/ns#" term="Sample Paper"/><title type='text'>Cbse Class 10th Mathamatics SA-II Sample Paper</title><content type='html'>&lt;center&gt;&lt;div&gt;


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