Professional Documents
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Catenation
Hydrocarbons
Haloalkanes
Alcohols
Aldehydes
Ketones
Carboxylic acids
CARBON AND ITS COMPOUNDS
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CARBON – is an element, non metal, and present in very small amount in atmosphere.
In Atmosphere – 0.02% and in Air - 0.03% as CO2 gas. All living things plants and animals are made up of
Self combination (catenation) – carbon can link or combine with one another by means of covalent
bonds to form long chains of carbon atom. This property is also called
Tetravalency - tetra means 4 and valency refers to valency. Valency of carbon is four(which is quite
large). Due to this a carbon atom can form large number of carbon atoms with a number of carbon
atoms as well as with a large number of other elements.
Types of hydrocarbons
1.
1. Hydrocarbons
Compounds made of hydrogen and carbon mainly are called Hydrocarbons.( Hydrogen + Carbon). Methane (CH 4),
Ethane(C2H6) etc. it is of two types.
Saturated Htdrocarbons – a hydrocarbon which is connected by only single bond.it is further divided into
one part.
By VIVEK MISHRA
i. Alkanes – a hydrocarbon in which the carbon atoms are connected by only by single
covalent bond. Methane (CH4),ethane (C2H6)
2. Unsaturated Hydrocarbons – the hydrocarbon in which two carbon atoms are connected by “Double bond”
or “Triple bond” . it is further divided into two parts.
ii. Alkenes – a hydrocarbon in which the two carbon atom are connected by a double bond. H 2
C=CH2 called ethane. CH3-CH=CH2 called as propane.
iii. Alkynes- a hydrocarbon in which the two carbon atoms are connected by a triple bond.
HC≡CH as ethyne.
ALKANES
a hydrocarbon in which the carbon atoms are connected by only by single covalent bond. Methane (CH 4),ethane
(C2H6).It’s general formula is CnH2n+2 .
A hydrocarbon in which the two carbon atom are connected by a double bond. H 2 C=CH2 called ethane. CH3-CH=CH2
called as propane. It’s general formula is CnH2n .
ALKYNES
A hydrocarbon in which the two carbon atoms are connected by a triple bond. HC≡CH is known as ethyne. Its
general formula is CnH2n-2 .
Homologous series – a group of organic compounds having similar structures and similar chemical properties in
which the every successive compound differ by CH2.. example
Functional Groups
Alkanes, Alkenes, and Alkynes are already discussed above. They are also the types of functional group.
CH3-OH methan+ol (“e” is removed from all alkane names) and becomes Methanol
1. Combustion:- (Burning) :- The process of burning of any carbon compounds in air to give carbon dioxide,
water, heat and light is known as combustion:
(a) Saturated hydrocarbons (alkanes) generally burn in air with a blue, now sooty flame.
(b) Unsaturated hydrocarbons (alkenes, alkynes) are burned in pure oxygen, then they will burn completely
producing a blue flame (without any smoke).
2. Substitution Reaction:- Reaction in which one or more hydrogen atoms of a hydrocarbon are replaced by
some other atoms( like chlorine).
Ethane
(Unsaturated) (Saturated)
Physical properties:
(ii) Lighter than water and miscible with liquid in all properties, because of presence of hydroxyl group in it. It is
neutral.
Chemical Properties:-
(1)Combustion:- Burning in the presence of oxygen. Ethanol is highly inflammable. On burning gives blue flame.
Ethanol as fuel:- Since ethanol burns with a clear flame giving a lot of heat, therefore, it is used as a fuel. It is also
used as an additive in petrol in courtiers like Brazil.
Conc.H2SO4; 1700C
Denatured Alcohol:- Ethyl alcohol which has been made unfit for drinking purposes by adding small amounts of
poisonous substances like methanol, pyridine, copper sulphate etc. (CuSO 4 imparts blue color when added with
ethanol.)
1. Sodium metal test:- add a small piece of sodium to the organic liquid taken in a dry test tube. If the
bubbles (or effervesces) of hydrogen gas are produced it indicates that the given liquid is Alcohol.
2C2H5OH + 2Na ----------------► 2C2H5-O-Na+ + H2.
2. Ester test for alcohol:- the organic compound is warmed with some glacial Ethanoic acid and a few drops
of concentrated sulphuric acid. A sweet smell (due to the formation of ester) indicates that the organic
compound is an alcohol.
USES OF ETHANOL
1.In the manufacture of paints, varnishes, lacquers, medicines, perfumes, dyes, soaps and synthetic rubber.
2.It is used as an organic solvent in laboratory.
3.It is also used as a fuel in the cars.
4.Ethyl alcohol is used in alcoholic beverages like wine, beer, whisky, and other liquors. Whisky (35%), wine
(10-20%), beer (6%) of ethanol.
5. It is also used as an antiseptic to sterilize the wounds and syringes in hospitals.
By VIVEK MISHRA carbon and its compounds
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Ethanoic acid(CH3COOH)
Common name – Acetic acid.A dilute solution of ethanoic acid in water is called vinegar.vinegar contains 5-8 % of
ethanoic acid.
1. Action on litmus:- ethanoic acid is acidic in nature. It turns blue litmus solution red. Dilute ethanoic acid
turns universalindicator paper to orange, showing that its pH is about 4.
2. Reaction with carbonates and hydrogencarbonates:- when it is added to carbonates and
hydrogencarbonates to evolve carbondioxide gas alongwith the formation of salt and water.
i. Reaction with sodium carbonate;- ethanoic acid reacts with sodium carbonate to form sodium
carbonate and carbondioxide gas.
2CH3-COOH + Na2CO3 ------------------►2CH3-COONa + H2O + CO2
Ethanoic acid ethyl ethanoate
ii. Reaction with sodium hydrogencarbonate:- it reats with sodium hydrogen carbonate to evolve brisk
effervenscence of carbondioxide.
CH3-COOH + NaHCO3 ------------------►CH3-COONa + H2O + CO2
Ethanoic acid ethyl ethanoate
3. Reaction with sodium hydroxide:- ethanoic acid reats with base to form salts and water. This is also the
example of neutralisation reaction .
CH3-COOH + NaOH ------------------►CH3-COONa + H2O
4. Reaction with alcohols: formation of esters:- ethanoic acid reacts with alcohols to form ester in the presence
of a little concentrated sulphuric acid.
Esters are generally volatile liquids having sweet smell or pleasant smell. They are also said to have fruity
smell. It is used as flavouring agents in ice creams, sweets and cold drinks. Esters can hydrolysed back to the
alcohol and carboxylic acid.
Hydrolysis of esters:- the alkalline hydrolysis of estersis known as saponification (Soap making).this reaction is used
for the preparation of soaps.when the esters of higher fatty acids with glycerolare hydrolysed with sodium hydroxide
solution, we get sodium salts of higher fatty acids which are called soaps.
1. Sodium hydrogencarbonate test:- the organic compounds is taken in a test tube and pinch of sodium
hydrogencarbonate is added to it. Evolution of carbondioxide gas with brisk effervescence shows that the
given organic compound is a carboxylic acid.
CH3-COOH + NaHCO3 ------------------►CH3-COONa + H2O + CO2
Ethanoic acid ethyl ethanoate
2. Ester test for acids:- the organic compound is warmes with some ethanol and 2-3 drops of concentrated
sulphuric acid. A sweet smell due to the formation of ester shows that the organic compound is carboxylic
acid.
3. Litmus test:- some blue litmus solution is added to the organic compound . if the blue litmus solution turns
red, it shows that the organic compound is acidicin nature hence carboxylic acid.
1. Silute ethanoic acid is used as a food preservative in the preparation of pickles and sauces . As a vinegar it is
also used as a appetiser for dressing food dishes.
2. Used for making cellulose acetatewhich is an important artificial fibre.
3. Used in the manufacture of acetone (propanone) and esters used in perfumes.
4. Ethanoic acid is used in the preparation of dyes, plastics and pharmaceuticals.
5. Used to coagulaterubber from latex.
Soaps
A soap is the salt (or potassium salt) of a long chain carboxylic acid (fatty acid) which has cleansing
propertise in water.examples of soaps are : sodium stearate and sodium palmitate.
i. Sodium stearate,C17H35COONa (made from stearic acid).
ii. Sodium palmitate,C15H31COONa (made from palmitic acid).
Soap solution turns red litmus to blue.
A soap molecule is made up of two parts: a long hydrocarbon part and a short ionic part containing
-COONa group . the soap molecule have a tadpole structure. When soap is dissolved in water, it forms a
colloidal suspension in water in which the soap molecules cluser together to form spherical micelles( a
speacial aggregate of soap molecule in the soap solution in water is called micelle).
The micelle formation takes place when soap is added to water because the hydrocarbon chains of soap
molecule are hydrophobic (water repelling) which are insolube in water, but the ionic ends of soap
molecule are hydrophillic (water attractiing) and hence soluble in water.
When a dirty cloth is put in water containing dissolved soap, the hydrocarbon ends forms the micellewith
the grease and oil particles present in the cloth and the ionic end of the soap molecule in the miclle
however remain attach to the water.when the dirty cloth is agitated in the soap solution , the oil and
greasy particles present on its surface and entrapped by soap micelles get dispersed In water due to which
the soap water becomes dirty but the cloth gets cleaned. The cloth is cleaned throughlyby rinsing in clean
water a number of times .
Limitations of soap
1. Hard water contains calcium and magnesium salts. Soap is not suitable for washing clothes with hard water
because a large amount of soap is used in reacting with the calcium and magnesium ions of hard water to
form insoluble precipitate called scum, before it can be used for real urposes of washing .
2. The scum(curdy precipitate) formed by the action of soap on hard water sticks to the clothes being washed
and interferes with the cleaning ability of the additional soap. This makes the cleansing of soap difficult.
Detergents
Detergents are called soap less soaps because though they act like a soap in having he cleansing properties, they do
not contain the usual soaps like sodium sterate.A detergent is the sodium salt of a long chain benzene sulphonic acid
which has cleansing propertise in water.