Which reagent can convert acetic acid into ethanol?
A.Na + alcohol
B. \[{H_2} + Pt\]
C. \[LiAl{H_4} + ether\]
D.Sn + HCl
Answer
589.8k+ views
Hint: In the presence of Sodium (Na), the acetic acid gives sodium salt of acetic acid. The reagent \[{H_2} + Pt\] is basically used for the hydrogenation. Aluminum lithium hydride \[\left( {LiAl{H_4}} \right)\] is a strong reducing agent and is able to reduce acids to alcohols.
Complete step by step answer:
Acetic acid \[\left( {C{H_3}COOH} \right)\] must undergo reduction to form ethanol \[\left( {{C_2}{H_5}OH} \right)\].
Aluminum Lithium hydride \[\left( {LiAl{H_4}} \right)\] is used as a reducing agent which reduces carbonyl compounds into alcohols. \[LiAl{H_4}\] can convert acetic acid into ethanol as it acts as a reducing agent and is capable of reducing carboxylic acids to alcohols.
\[C{H_3}COOH\xrightarrow{{LiAl{H_4} + ether}}C{H_3}C{H_2}OH\]
acetic acid ethanol
So, when acetic acid is treated with aluminum lithium hydride \[\left( {LiAl{H_4}} \right)\] in the presence of ether followed by the hydrolysis in acidic medium yields ethanol as a product.
While when we see other options given in the question and the reason these reagents cannot convert acetic acid into ethanol because,
Reagent Na + alcohol: The acetic acid in the presence of Sodium (Na) gives sodium salt of acetic acid.
Reagent \[{H_2} + Pt\]: Molecular Hydrogen \[\left( {{H_2}} \right)\] and a catalyst like nickel (Ni), Palladium (Pd) or platinum (Pt) is basically used for the hydrogenation.
Reagent Sn + HCl: Sn + HCl can reduce the nitro group but it is not capable of reducing the carbonyl group.
So, \[LiAI{H_4} + ether\], is the reagent that can convert acetic acid into ethanol
Therefore, the correct answer is option (C).
Note: Aluminum lithium hydride or LAH, is an inorganic compound having the chemical formula \[LiAl{H_4}\] and it is a grey solid. This compound is commonly used as a reducing agent in organic synthesis, especially for the reduction of esters, carboxylic acids, and amides.
Complete step by step answer:
Acetic acid \[\left( {C{H_3}COOH} \right)\] must undergo reduction to form ethanol \[\left( {{C_2}{H_5}OH} \right)\].
Aluminum Lithium hydride \[\left( {LiAl{H_4}} \right)\] is used as a reducing agent which reduces carbonyl compounds into alcohols. \[LiAl{H_4}\] can convert acetic acid into ethanol as it acts as a reducing agent and is capable of reducing carboxylic acids to alcohols.
\[C{H_3}COOH\xrightarrow{{LiAl{H_4} + ether}}C{H_3}C{H_2}OH\]
acetic acid ethanol
So, when acetic acid is treated with aluminum lithium hydride \[\left( {LiAl{H_4}} \right)\] in the presence of ether followed by the hydrolysis in acidic medium yields ethanol as a product.
While when we see other options given in the question and the reason these reagents cannot convert acetic acid into ethanol because,
Reagent Na + alcohol: The acetic acid in the presence of Sodium (Na) gives sodium salt of acetic acid.
Reagent \[{H_2} + Pt\]: Molecular Hydrogen \[\left( {{H_2}} \right)\] and a catalyst like nickel (Ni), Palladium (Pd) or platinum (Pt) is basically used for the hydrogenation.
Reagent Sn + HCl: Sn + HCl can reduce the nitro group but it is not capable of reducing the carbonyl group.
So, \[LiAI{H_4} + ether\], is the reagent that can convert acetic acid into ethanol
Therefore, the correct answer is option (C).
Note: Aluminum lithium hydride or LAH, is an inorganic compound having the chemical formula \[LiAl{H_4}\] and it is a grey solid. This compound is commonly used as a reducing agent in organic synthesis, especially for the reduction of esters, carboxylic acids, and amides.
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