91Ó°ÊÓ

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

${\mathrm{CH}}_3-\mathrm{CH}\left({\mathrm{CH}}_3\right)-{\mathrm{CH}}_2-\mathrm{OH}(2-\mathrm{Methyl}-\mathrm{propanol})$

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, ${\mathrm{CH}}_3-\mathrm{CH}\left({\mathrm{CH}}_3\right)-{\mathrm{CH}}_2-\mathrm{OH}(2-\mathrm{Methyl}-\mathrm{propane}-1-\mathrm{ol})$is a primary alcohol. Hence, it is oxidized to ${\mathrm{CH}}_3-\mathrm{CH}\left({\mathrm{CH}}_3\right)-\mathrm{CHO}(2-\mathrm{Methyl}-\mathrm{propanal})$.

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

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

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

Given, ${\mathrm{CH}}_3-{\mathrm{CH}}_2-\mathrm{C}\left({\mathrm{CH}}_3\right)\mathrm{OH}-{\mathrm{CH}}_3(2-\mathrm{Methyl}-\mathrm{butane}-2-\mathrm{ol})$is a tertiary alcohol. Hence, no oxidation will take place.

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

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

Given, Cyclobutanol is a secondary alcohol. Hence, it is oxidized to Cyclobutanone.

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

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

Given, ${\mathrm{CH}}_3-\mathrm{CH}\left({\mathrm{CH}}_3\right)-{\mathrm{CH}}_2-\mathrm{CH}\left(\mathrm{OH}\right)-{\mathrm{CH}}_3(4-\mathrm{Methylpentane}-2-\mathrm{ol})$is a secondary alcohol. Hence, it is oxidized to ${\mathrm{CH}}_3-\mathrm{CH}\left({\mathrm{CH}}_3\right)-{\mathrm{CH}}_2-\mathrm{CO}-{\mathrm{CH}}_3(4-\mathrm{Methylpentane}-2-\mathrm{one})$.