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Question : 34
Total: 39
(A) (i) Draw the structure of the following compounds:
(a) Butanoic acid
(b) Chloropentane
(ii) How are structure (i) and structure (ii) given below related to one another? Give reason to justify your answer.
(iii) Differentiate between saturated and unsaturated carbon compounds on the basis of their general formula.
OR
(B) (i) What happens when a small piece of sodium is dropped in ethanol? Write the equation for this reactions.
(ii) Why is glacial acetic acid called so?
(iii) What happens when ethanol is heated at443 K in the presence of conc. H 2 SO 4 ? Write the role of conc. H 2 SO 4 in this case.
(iv) Write an equation showing saponification.
(a) Butanoic acid
(b) Chloropentane
(ii) How are structure (i) and structure (ii) given below related to one another? Give reason to justify your answer.
Draw one more possible structure for above case.
(iii) Differentiate between saturated and unsaturated carbon compounds on the basis of their general formula.
OR
(B) (i) What happens when a small piece of sodium is dropped in ethanol? Write the equation for this reactions.
(ii) Why is glacial acetic acid called so?
(iii) What happens when ethanol is heated at
(iv) Write an equation showing saponification.
Solution:
(A) (i) (a) H −
−
−
−
− OH
(b)H −
−
−
−
−
− H
(ii) Both are isomers of compound with chemical formulaC 6 H 14 . Structure (i) is 2,3-dimethylbutane whileStructure (ii) is 2,2-dimethylbutane. One more isomer is, 3-methylpentane.
CH 3 − CH 2 −
H − CH 2 − CH 3
(iii) Saturated carbon compounds always follow the general formula of C n H 2 n + 2 . In case of unsaturated carbon compounds, they always follow the general formula C n H 2 n if there is a carbon-carbon double bond and formula C n H 2 n − 2 if there is a carbon-carbon triple bond.
OR
(B) (i) Alcohols react with sodium leading to the evolution of hydrogen.
2 Na + 2 CH 3 CH 2 OH →
+ H 2 ↑
(ii) The melting point of pure ethanoic acid is 290 K and hence it often freezes during winter in cold climates. This gave rise to its name glacial acetic acid.
(iii) Heating ethanol at443 K with excess concentrated sulphuric acid results in the dehydration of ethanol to give ethene. In this case, concentrated sulphuric acid act as a dehydrating agent as at removes water from ethanol.
ethanol.
CH 3 − CH 2 OH
CH 2 = CH 2 + H 2 O
(iv) On treating with sodium hydroxide, which is an alkali, the ester is converted back to alcohol and sodium salt of carboxylic acid. This reaction is known as saponification because it is used in the preparation of soap. Soaps are sodium or potassium salts of long chain carboxylic acid.
CH 3 COOC 2 H 5
C 2 H 5 OH + CH 3 COONa
(b)
(ii) Both are isomers of compound with chemical formula
OR
(B) (i) Alcohols react with sodium leading to the evolution of hydrogen.
(iii) Heating ethanol at
ethanol.
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