
How will you obtain:
$ \left( 1 \right) $ Formic acid from Acetic acid
$ \left( 2 \right) $ Acetaldehyde from Acetylene
Answer
546.6k+ 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
Why are manures considered better than fertilizers class 11 biology CBSE

Find the coordinates of the midpoint of the line segment class 11 maths CBSE

Distinguish between static friction limiting friction class 11 physics CBSE

The Chairman of the constituent Assembly was A Jawaharlal class 11 social science CBSE

The first National Commission on Labour NCL submitted class 11 social science CBSE

Number of all subshell of n + l 7 is A 4 B 5 C 6 D class 11 chemistry CBSE

Trending doubts
Differentiate between an exothermic and an endothermic class 11 chemistry CBSE

10 examples of friction in our daily life

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

Difference Between Prokaryotic Cells and Eukaryotic Cells

State the laws of reflection of light

Explain zero factorial class 11 maths CBSE

