Question

Draw the condensed structural or line-angle formula for the aldehyde or ketone formed when each of the following alcohols is oxidized [O] (if no reaction, write none):

Short answer

a. Propanal

b. Hexane$-2-$one

c. Cyclohexanone

d. $2,3-$dimethyl-pentanal

Step-by-step solution

Part(a) Step 1: Given information 

We need to draw the condensed structural or line-angle formula for the aldehyde or ketone formed when following alcohol is oxidized:

${\mathrm{CH}}_3-{\mathrm{CH}}_2-{\mathrm{CH}}_2-\mathrm{OH}$

Part(a) Step 2: Explanation

Alcohols are converted to aldehydes and ketones during the oxidation process. This is one of the most crucial reactions in organic chemistry. When primary alcohols are oxidised, aldehydes and carboxylic acids are generated; when secondary alcohols are oxidised, ketones are formed. Tertiary alcohols, on the other hand, can't be oxidised without destroying the molecule's C–C bonds.

Given, ${\mathrm{CH}}_3-\mathrm{CH}\left(\mathrm{OH}\right)-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_3$(Propanol) is a primary alcohol. Hence, it is oxidized to ${\mathrm{CH}}_3-\mathrm{CO}-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_3$(Propanal).

Part(b) Step 1: Given information 

We need to draw the condensed structural or line-angle formula for the aldehyde or ketone formed when following alcohol is oxidized:

${\mathrm{CH}}_3-\mathrm{CH}\left(\mathrm{OH}\right)-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_2-{\mathrm{CH}}_3$

Part(b) Step 2: Explanation

When primary alcohols are oxidised, aldehydes and carboxylic acids are generated; when secondary alcohols are oxidised, ketones are formed. Tertiary alcohols, on the other hand, can't be oxidised without destroying the molecule's C–C bonds.

Given, (Hexane$-2-$ol) is a secondary alcohol. Hence, it is oxidized to (Hexane$-2-$one).

Part(c) Step 1: Given information 

We need to draw the condensed structural or line-angle formula for the aldehyde or ketone formed when following alcohol is oxidized:

Part(c) Step 2: Explanation

When primary alcohols are oxidised, aldehydes and carboxylic acids are generated; when secondary alcohols are oxidised, ketones are formed. Tertiary alcohols, on the other hand, can't be oxidised without destroying the molecule's C–C bonds.

Given, Cyclohexanol is oxidized to give Cyclohexanone.

Part(d) Step 1: Given information 

We need to draw the condensed structural or line-angle formula for the aldehyde or ketone formed when $2,3-$dimethyl-pentanol is oxidized.

Part(d) Step 2: Explanation

When primary alcohols are oxidised, aldehydes and carboxylic acids are generated; when secondary alcohols are oxidised, ketones are formed. Tertiary alcohols, on the other hand, can't be oxidised without destroying the molecule's C–C bonds.

Given, $2,3-$dimethyl-pentanol is oxidized to $2,3-$dimethyl-pentanal.