
How will you obtain:
$ \left( 1 \right) $ Formic acid from Acetic acid
$ \left( 2 \right) $ Acetaldehyde from Acetylene
Answer
549.6k+ views
Hint: For in this conversion we use too many methods and can be converted into a desired product by various steps. For example, to obtain the formic acid from acetic acid. There are three steps for this conversion. Which we will discuss in complete solution:
Complete step by step answer:
In the given question there are two conversions. Let's solve one by one.
$ \left( 1 \right) $ For the conversion of acetic acid to formic acid. This conversion can be done by many methods.
Method $ 1 $ :
Step $ 1 $ : Reaction of acetic acid with sodium azide gives out methylamine. This reaction is known as Schmidt reaction
$ C{H_3}COOH + Na{N_3} \to N{H_2}C{H_3} $
Step $ 2 $ : Reaction of methylamine with $ HN{O_2} $ to give out methanol
$ N{H_2}C{H_3} + HN{O_2} \to C{H_3}OH $
Step $ 3 $ : Oxidation of methanol via potassium dichromate in the presence of acid to give formic acid.
$ C{H_3}COOH\xrightarrow[{{H_ + }}]{{{K_2}Cr{O_7}}}HCOOH $
$ \left( 2 \right) $ For conversion of acetaldehyde from acetylene. Acetylene can be converted into acetaldehyde in a single step process or multi steps.
Method $ 1 $ : (single step process)
Reaction of acetylene with water in presence of sulphuric acid and mercury sulphate to give acetaldehyde.
$ {C_2}{H_4} + {H_2}O\xrightarrow[{HgS{O_4}}]{{{H_2}S{O_4}}}C{H_3}CHO $
This reaction is known as the Kucherov reaction.
Method $ 2 $ : (Multi steps process)
Step $ 1 $ : Acetylene reacts with lithium aluminium hydride to give Ethane.
$ {C_2}{H_4}\xrightarrow{{LiAl{H_4}}}C{H_3}C{H_3} $
Step $ 2 $ : Ethane reacts with chlorine in presence of sunlight to give out chloroethane
$ C{H_3}C{H_3} + C{l_2}\xrightarrow{{Sunlight}}C{H_3}C{H_2}Cl $
Step $ 3 $ : Reaction of chloroethane with aqueous potassium hydroxide to give out ethanol and then ethanol react with $ PCC $ to produce acetaldehyde.
$ C{H_3}C{H_2}Cl + Aq.KOH \to {C_2}{H_5}OH $
$ {C_2}{H_5}OH + PCC \to C{H_3}CHO $ .
Note:
For the conversion of acetaldehyde from acetylene if we take methyl acetylene as a reactant in Kucherov reaction then the resultant product is propanal. If the alkynes are highly substituted then we will get ketone as the product.
Complete step by step answer:
In the given question there are two conversions. Let's solve one by one.
$ \left( 1 \right) $ For the conversion of acetic acid to formic acid. This conversion can be done by many methods.
Method $ 1 $ :
Step $ 1 $ : Reaction of acetic acid with sodium azide gives out methylamine. This reaction is known as Schmidt reaction
$ C{H_3}COOH + Na{N_3} \to N{H_2}C{H_3} $
Step $ 2 $ : Reaction of methylamine with $ HN{O_2} $ to give out methanol
$ N{H_2}C{H_3} + HN{O_2} \to C{H_3}OH $
Step $ 3 $ : Oxidation of methanol via potassium dichromate in the presence of acid to give formic acid.
$ C{H_3}COOH\xrightarrow[{{H_ + }}]{{{K_2}Cr{O_7}}}HCOOH $
$ \left( 2 \right) $ For conversion of acetaldehyde from acetylene. Acetylene can be converted into acetaldehyde in a single step process or multi steps.
Method $ 1 $ : (single step process)
Reaction of acetylene with water in presence of sulphuric acid and mercury sulphate to give acetaldehyde.
$ {C_2}{H_4} + {H_2}O\xrightarrow[{HgS{O_4}}]{{{H_2}S{O_4}}}C{H_3}CHO $
This reaction is known as the Kucherov reaction.
Method $ 2 $ : (Multi steps process)
Step $ 1 $ : Acetylene reacts with lithium aluminium hydride to give Ethane.
$ {C_2}{H_4}\xrightarrow{{LiAl{H_4}}}C{H_3}C{H_3} $
Step $ 2 $ : Ethane reacts with chlorine in presence of sunlight to give out chloroethane
$ C{H_3}C{H_3} + C{l_2}\xrightarrow{{Sunlight}}C{H_3}C{H_2}Cl $
Step $ 3 $ : Reaction of chloroethane with aqueous potassium hydroxide to give out ethanol and then ethanol react with $ PCC $ to produce acetaldehyde.
$ C{H_3}C{H_2}Cl + Aq.KOH \to {C_2}{H_5}OH $
$ {C_2}{H_5}OH + PCC \to C{H_3}CHO $ .
Note:
For the conversion of acetaldehyde from acetylene if we take methyl acetylene as a reactant in Kucherov reaction then the resultant product is propanal. If the alkynes are highly substituted then we will get ketone as the product.
Recently Updated Pages
The number of solutions in x in 02pi for which sqrt class 12 maths CBSE

Write any two methods of preparation of phenol Give class 12 chemistry CBSE

Differentiate between action potential and resting class 12 biology CBSE

Two plane mirrors arranged at right angles to each class 12 physics CBSE

Which of the following molecules is are chiral A I class 12 chemistry CBSE

Name different types of neurons and give one function class 12 biology CBSE

Trending doubts
One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

What is 1s 2s 2p 3s 3p class 11 chemistry CBSE

Discuss the various forms of bacteria class 11 biology CBSE

State the laws of reflection of light

Explain zero factorial class 11 maths CBSE

An example of chemosynthetic bacteria is A E coli B class 11 biology CBSE

