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Saturday, November 23, 2013

Soaps - preparation of soaps - Detergents - advantages and disadvantages

10th Chemistry : Soaps and Detergents [Carbon and Its Compound]
 SOAPS
Metallic salts prepared from natural fats are called soaps. Soap is a sodium salt or potasium salt of long chain fatty acids that has cleansing action in water. Sodium stearate, sodium oliate and sodium  palmitate are some examples of soaps.

Stearic acid is a long chain fatty acid. Its formula is C17H35COOH. This reacts with sodium hydroxide to give a compound called sodium stearate, which has properties of soap.

Similarly, sodium hydroxide reacts with oleic acid and palmitic acid forming sodium oleate   (C17H33COONa) and sodium palmitate (C17H31COONa) respectively.
Please Note!
Fatty acids are organic compounds. The molecules of these compounds contain a carboxyl  group                 {-COOH}. These molecules react with a trihydric alcohol called glycerol to form a class of compounds called esters.
Groundnut oil, coconut oil, palm oil, caster oil, gingely oil, animal fat etc are all esters of fatty acids. Fats and fatty oils are called glyceryl esters or tglycerides.

PREPARATION OF SOAP
Experiment : Take about 30 ml of a vegetable oil in a beaker. Add about 60ml of 20% sodium hydroxide solution to it. Heat slowly until the mixture boils. After 5-10 minutes of boiling, add about 5g of sodium chloride to separate soap from the solution. Cool the solution. Observe the creamy layer of soap floating on the  solution.
We need animal fat or vegetable oil, sodium hydroxide and sodium chloride for preparing soap. Fat or vegetable oil is a glyceride or a glyceryl ester. Soap is prepared by hydrolyzing fat or oil with bases such as sodium hydroxide or potassium hydroxide. This process of preparing soap is called saponification.
When a mixture of a oil/fat and a strong solution of sodium hydroxide is boild in an iron tank, a sodium salt of the fatty acid and glycerol are formed. The sodium salt of the fatty acid thus formed is nothing but soap.

Please Note!
A Swedish chemist, Carl Wilhelm Scheel, discovered accidentally the process of preparation of soap in 1783. He boiled olive oil with lead oxide and obtained a sweetish substance which was seat to taste. This substance is now known as glycerine.

Oil/fat + sodium hydroxide ----->  soap + glycerol

                                   Fig-01
Please Note! 
Glycerol
Glycerol is a sweet viscous liquid soluble in water. It is a byproduct of saponification process. It is commonly called glycerine. Its formula is CH2OH.CHOH.CH2OH. It is used in the manufacture of explosives, plastics, and pharmaceuticals. It is also used to prevent freezing.

Soap thus formed is separated with the help of sodium chloride. Addition of sodium chloride reduces the solubility of soap considerable. Soap, being lighter, floats like a cream on the solution. It is separated from the solution; suitable chemicals of suitable colour and odour are added to it and cast into moulds. When soap cools and solidifies, it is cut into desired shapes and packed. Glycerol exists in dissolved state in the solution. It is separated by distillation.

How does soap clean
Soap dissolves in water. This is due to the contrasting properties of the ends of the soap molecules.
A soap molecule has a long hydrocarbon end [E.g. CH3(CH2)16] and a short ionic end containing COONa+.  The non-ionic hydrocarbon end has the property to repel water. The other end, which is ionic, has the property to attract water. This end attaches itself to water. The hydrocarbon end attaches to the dirt or grease to form structures called ‘micelles’.

                                                                           Figure-02
In micelles soap molecules are arranged radially. The end attached to water pulls out the dirt from the fabric. This can be washed off with water.

DETERGENTS
The term detergent is derived from a Latin word which means surface active. Synthetic detergents are commonly known as detergents. Detergents are also called soap less soaps.

Detergents do not form insoluble ‘scum’ with magnesium and calcium ions present in hard water. Therefore, detergents clean better than soap even in hard water.

Detergents are sodium salts of long chain benzene sulphonic acid or sodium salts of long chain alkyl hydrogen sulphate. A detergent molecule consists of a large hydrocarbon group that is non-ionic and a sulphonate (SO3- Na+) or a sulphate (SO4- Na+)  group that is ionic. Sodium n-dodecyl benzene sulphonate and Sodium dodecyl sulphate are two well-known detergents.

Note:
Long chain hydrocarbons obtained from petroleum are treated with concentrated sulphuric acid. The organic acids produced during this process are neutralized with sodium hydroxide. The sodium salt obtained is a detergent.

ADVANTAGES OF DETERGENTS OVER SOAPS
Detergents have more advantages than soap. Therefore, detergents are more widely used than soap. Let us now turn our focus towards the advantages of detergents.

! Detergents cleanse well even in hard water. Soap is not so good for washing when water is hard.

! Detergents are made from hydrocarbons obtained from petroleum. Soap is prepared from vegetable oil or animals fat that are usually edible. Detergents are not bio-degradable. Soaps are biodegradable.

! Detergents cleanse well even in acidic medium. Soap does not cleanse well in such a medium.

Detergents have their disadvanges.

! Detergents are not bio-degradable. They polutes water and soil.

Total Fatty Matter (TFM)
 Soaps are graded in terms of total fatty matter or TFM. Bureau of Indian Standards (BIS) has catogorised bath or toilet soaps as ‘normal’, ‘baby,  transparent, and antibacterial soaps. The last three are called specialty soaps  targeted to specific users. A toilet soap is a cosmetic by law and it must fulfil the  requirements of the relevant Indian standard.

 T. F. M or total fatty matter is a measure for identifying the amount of fatty matter  present in soaps. TFM of a sample of soap can be determined as follows. A known  weight of the soap is dissolved in water and the solution is treated with dilute  sulphuric acid. The soap decomposes to sodium suplphate and fatty acids. The fatty acids so formed can be estimated. From this TFM can be calculated. On the  basis TFM, toilet soaps can be classified into three grades.  

Grade
 TFM
Moisture
Free salt (NaCl)
I
above 80
Max :
13.5
Max :
0.7
II
65 – 80

13- 15

0.8
III
55- 65

15-20

1.5


Q. Swapnesh, living in Ooty, was washing clothes in cold water. He found that  the clothes were not getting clean. Geeta , his niece, suggested that he wash  the clothes in warm water. Washing of clothes with soaps or detergents is  easier in Luke warm water than cold water.
(a)Why?
(b) What value do you derive from this?
Ans:
(a) Action of soaps is due to formation of micelles. But the formation of micelles takes place at a minimum temperature called ‘Kraft  temperature’. This temperature is reached in lukewarm water.
(b) Be humble to accept a scientific fact from a younger person 

Wednesday, November 20, 2013

Properties of Alkanes/ Alkenes/ Alkynes (10th Carbon and its compounds) CBSE_NCERT Class Xth

10th Carbon and its compounds_ CBSE_NCERT Class Xth 

(a) Alkanes are gas (C1to C4) ; liquid (C5to C17) and rest are solid at room temperature.


(b) The melting and boiling point of Alkanes increases with increase in number  of C  – atom in Alkanes .
Alkane
Formula
Boiling point [°C]
Melting point [°C]
State (at 20 °C)
Methane
CH4
-162
-182
gas
Ethane
C2H6
-89
-183
gas
Propane
C3H8
-42
-188
gas
Butane
C4H10
0
-138
gas
Pentane
C5H12
36
-130
liquid
Hexane
C6H14
69
-95
liquid
Heptane
C7H16
98
-91
liquid
Octane
C8H18
126
-57
liquid
Nonane
C9H20
151
-54
liquid
Decane
C10H22
174
-30
liquid
Undecane
C11H24
196
-26
liquid
Dodecane
C12H26
216
-10
liquid
Hexadecane
C16H34
281
18
liquid
Icosane
C20H42
343
37
solid
Triacontane
C30H62
450
66
solid
Tetracontane
C40H82
525
82
solid
Pentacontane
C50H102
575
91
solid
Hexacontane
C60H122
625
100
solid
Source: http://en.wikipedia.org/wiki/Alkane

Reason: 
Alkanes experience inter-molecular van der Waals forces. Stronger inter-molecular van der Waals forces give rise to greater boiling points of alkanes.

A straight-chain alkane will have a boiling point higher than a branched-chain alkane due to the greater surface area in contact.  


Note:  In Chemistry the Van der Waals forces include attractions and repulsions between atoms, molecules, and surfaces, as well as other intermolecular forces.

 (c) The density of the alkanes usually increases with increasing number of carbon atoms

Alkane
Formula
Density
Pentane
C5H12
0.626 (liquid)
Hexane
C6H14
0.659 (liquid)
Heptane
C7H16
0.684 (liquid)
Octane
C8H18
0.703 (liquid)
Nonane
C9H20
0.718 (liquid)

(d) Alkanes are generally insoluble in polar compound like water but dissolve in organic solvents (Non polar compound) like benzene. The liquid alkanes are good solvents for many other covalent compounds.
Reason: Alkanes do not conduct electricity, nor are they polarized by electricity. For this reason they do not form hydrogen bonds and are insoluble in polar solvents such as water.

(e) Alkanes are stable and less reactive than alkenes

Reason: This is because saturated hydrocarbons contain only single bonds which are very stable and difficult to break. On the other hand, unsaturated hydrocarbons contain pie bonds, which can be easily broken as they are more strained.

(f) Alkanes are generally good combustible material due presence of the good percentage of Hydrogen.

Since Alkanes burn with non smoky and non sooty flame due to presence of the good percentage of Hydrogen, It is used as a fuel like LPG and CNG

2CH4   +          2O2                 →        CO2    +          H2O    +          Heat
2C2H6  +          7O2                  →        4CO2   +          6H2O  +          Heat

However, if the supply of air or oxygen is not sufficient for complete combustion, carbon monoxide is formed. Carbon monoxide (CO) is highly poisonous.

2CH4              +          3O2      →                    2CO    +          4H2O
2C4H10           +         9O2      →                    8CO    +         10H2O

(g) Alkanes do not undergo addition reaction due to strong van der wall force.

Unlike alkane, generally  alkene Undergo  addition reaction with hydrogen gas in the presence of Polladium catalyst  and gives saturated hydrocarbon



Pd

CH2     =    CH2
+
H2
--------------->
CH3    -   CH3

ThIs addition reaction of hydrogen is helpful in converting vegetable Oil into saturated fat like vanaspati  gee . This reaction is commonly called Hydrogenation of Oil.

Note: Butter contain saturated compound where as cooking oil contain unsaturated compound. If Alkaline KMno4 added to both, pink color of KMno4 disappear in cooking oil but remain in pink in butter.



Ni

Vegetable Oil
+
H2
------------>
CH3    -   CH3  

(h)  Alkanes undergo addition reaction because hydrogen attached to carbon easily replaced by atom more reactive than hydrogen like halo atom Cl,Br ,I etc.




Sunlight



CH4    
 +
Cl2
------------>
CH3Cl
+
HCl 










Sunlight



 CH4Cl    
 +
Cl2
------------>
CH2Cl2
+
HCl 










Sunlight



CH2Cl2
 +
Cl2
------------>
CHCl3
+
HCl 










Sunlight



CHCl3
 +
Cl2
------------>
CH3Cl
+
HCl 

If chlorine present in excess , then reaction does not stopin between but keep on reacting till it form carbon tetra chloride

Bromine and chlorine react with alkene to form vicinal dihalides (iodine does not undergo addition reaction under normal conditions).




      CCl4



CH2 = CH2
+    
Cl2
----------->
CH2
-
CH2




 I

 I




Br

Br
Ethene



 1,2-Dibromoethane

CH2 = CH2
+    
Cl2
 -------->
CH3
-
CH
-
CH2






 I

 I






Cl

Cl
Ethene



       1,2-Dibropropane

Note: In Alkanes, the four valencies of carbon atom are saturated and they have stable s (sigma) bonds. Any nuleophile comes, one hydrogen atom is replaced to accommodate the nucleophile.

A nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.

e.g. CH4 + Cl2   --------> CH3Cl + HCl

In case of Alkene or Alkyne, Carbon atom has double or triple bonds. In this, one is stable s (sigma)  bond and the rests are unstable(or weak) p  bonds. When nucleophile approches to the carbon atom that has double or triple bonds, they easily break to accommodate it.
e.g., H2C=CH2 + Cl2  --------> H2ClC-CH2Cl.

(i) Cracking (or pyrolysis):  Higher alkanes undergo thermal decomposition to give lower alkanes. This process is called pyrolysis or cracking. In this process, vapour of higher alkanes is passed through a hot metal tube (5000C – 7000C). Propane on cracking gives,

     
D

C3H6 + H2
C3H8
------------>



CH4 + C2H4
Cracking of hexane gives butane and ethane.


D

C6H14
------------->
C4H10 + C2H4

Q. What's the difference between cracking and pyrolysis?

Pyrolysis : The decomposition of a compound on heating in absence of air is known as pyrolysis.

Cracking: is the breakdown of large organic compounds by use of a catalyst and low temperature to form fewer different compounds

Q.  In cracking will the decomposed hydrocarbon always be a saturated and a unsaturated hydrocarbons? Can they both be either unsaturated or saturated hydrocarbons?

Cracking is defined as the process of breaking or decomposition of large hydrocarbons into smaller compounds. This process is widely used in the petroleum industry. Usually, we get a mixture of alkane and alkenes by the process of cracking of hydrcarbons. This is because the bonds in the hydrocarbons can be cleared in any way. As a result, we will not get alkane and alkene exclusively but a mixture of both.
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X + energy → X+ + e-     Know your chemistry knowledge
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