Is it possible to oxidise t – butyl alcohol using acidified dichromate to form a carbonyl compound.

Can we use nucelophiles such as NH₃,CH₃O ^- for the Nucleophilic substitution of alcohols

Arrange the following in the increasing order of their boiling point and give a reason for your ordering
(i) Butan – 2- ol, Butan -1-ol, 2 –methylpropan -2-ol
(ii) Propan -1-ol, propan -1,2,3-triol, propan -1,3 – diol, propan -2-ol

Predict the major product, when 2-methyl but -2-ene is converted into an alcohol in each of the following methods.
(i) Acid catalysed hydration
(ii) Hydroboration
(iii) Hydroxylation using Baeyer's reagent

What is the major product obtained when two moles of ethyl magnesium bromide is treated with methyl benzoate followed by acid hydrolysis.

Suggest a suitable reagent to prepare secondary alcohol with identical group using Grignard reagent.

Draw the major product formed when 1-ethoxyprop-1-ene is heated with one equivalent of HI.

Identify the product (s) is / are formed when 1 – methoxy propane is heated with excess HI. Name the mechanism involved in the reaction.

Arrange the following in the decreasing order of order of acid strength.

Which of the following does not give iodoform reaction?

What happens when crotonaldehyde is reduced in the presence of LiAlH₄?

What happens when anisole is nitrated?

Why sodium metal cannot be used to dry alcohols but it can be used to dry ethers?

Identify the product A and B.

Identify the product C and D.