Primary alcohol can easily be prepared from primary alky `1` halide `via S_(N)2`reaction with aqueous `NaOH`. However, similar method does not work for the perparation tertiary acholo (tertiary butanol) from tertiary buty`1` bromide except?

How will you prepare Secondary, Tertiary, primary alcohol from Grignard reagent ?

Write equations for the steps in S_(N)1 mechanism of conversion of tertiary butyl bromide into tertiary butyl alcohol.

In S_(N^1) reactions, primary alkyl halides are more reactive than tertiary alkyl halides.

Write steps involved in S_(N)1 mechanism to the conversion of tertiary butyl bromide into tertiary butyl alcohol and mention its order.

Alcohols undergo acid catalysed elimination reactions to produce alkenes. Because water is lost in the elimination , this reaction is called dehydration reaction. Secondary and tertiary alcohols always give E1 reaction in dehydration. Primary alcohols whose beta -carbon is branched also give E1 reaction. The reactivity of alcohol for elimination reaction is tertiary alcohol gt secondary school gt Primary alcohol. Identify the product in the given reaction :

Which of the following chemical tests can be used to distinguish primary . Secondary and tertiary alcohol from each other ?

Which of the following chemical tests can be used to distinguish primary . Secondary and tertiary alcohol from each other ?