Identifying Compound (A)
The molecular formula of compound (A) is C6H12O2, which could be either a carboxylic acid or an ester. Upon reduction with LiAlH4, it gives two compounds, indicating the presence of both a carboxyl group and an ester group in compound (A). The most likely structure of compound (A) is ethyl acetate (CH3COOCH2CH3).
Most likely structure of compound (A): CH3COOCH2CH3 or CH3CH2COOCH3
Identifying Compound (B)
Upon reduction with LiAlH4, compound (A) gives compound (B), which is likely ethanol (CH3CH2OH).
Compound (B): CH3CH2OH
Identifying Compound (C)
Upon reduction with LiAlH4, compound (B) (acetaldehyde) gets reduced to propyl alcohol (CH3CH2CH2OH). LiAlH4 is a strong reducing agent, typically used to reduce aldehydes to primary alcohols.
Compound (C): CH3CH2CH2OH
Identifying Compound (D)
Compound (B) is ethanol (CH3CH2OH). When ethanol is oxidized using PCC (Pyridinium chlorochromate), it is converted to acetaldehyde (CH3CHO). This reaction is typical for primary alcohols, where mild oxidants like PCC prevent further oxidation to carboxylic acids.
Compound (D): CH3CHO
Identifying Compound (E)
Upon catalytic hydrogenation of acetaldehyde (CH3CHO), acrolein (CH3CH=CHCHO) is formed. This reaction involves the reduction of the carbonyl group in acetaldehyde into an alkene group while keeping the aldehyde functional group intact.
Compound (E): CH3CH=CHCHO
Identifying Compound (F)
Upon further oxidation of acrolein (CH3CH=CHCHO), acetic acid (CH3COOH) is produced. This is a common reaction where aldehydes undergo oxidation to form carboxylic acids.
Compound (F): CH3COOH