Alcohols, Phenols and Ethers
$$HBr$$ reacts fastest with:
The compound that will react with $$HBr$$ most readily is:
Reactivity order of alcohols with HBr is 3∘>2∘>1∘ alcohol.
The option (A) is a 3∘ alcohol and hence it will react most readikly with HBr.
Phenol (option D) does not react with HBr. (Ar-O) bond is not broken unless the ring is activated by the presence of electron withdrawing group (e.g., NO2) at o- and p-positions.
$$HBr$$ reacts fastest with:
Distinction between primary, secondary and tertiary alcohol is done by
The compound ‘A’ when treated with ceric ammonium nitrate solution gives yellow ppt. The compound ‘A’ is
In reaction of alcohols with alkali metal, acid etc. Which of the following alcohol will react fastest?
The starting substance for the preparation of $$CH_3I$$ is
Which of the following is responsible for iodoform reaction
t-butyl alcohol reacts less rapidly with metallic sodium than the primary alcohol. Explain why?
The group reagent for the test of alcohol is:
State whether the following statement is True or False. Methyl alcohol gives iodoform test.
State whether the following statement is True or False. $$FeSO_4+H_2O_2$$ is called Fenton's reagent.