Identify the nucleophile that attacks the carbocation in the second s – McqOptions

MCQOPTIONS

1.	Identify the nucleophile that attacks the carbocation in the second step of acid catalysed hydration of alkenes?
A.	OH–
B.	H2O
C.	H+
D.	H3O+
Answer» C. H+

Discussion

No Comment Found

Related MCQs

Which of the following aldehydes can produce 1o alcohols when treated with Grignard reagent?
Hydrolysis of the adduct formed form the reaction of ________ with methyl magnesium bromide gives 2-Methylpropan-2-ol.
Esters on catalytic hydrogenation always give a mixture of two different alcohols.
Which carbonyl compound yields secondary alcohols when treated with LiAlH4?
What happens when an aldehyde is treated with lithium aluminium hydride?
Propan-2-ol can be prepared form the hydroboration-oxidation of propene.
Which of the following is not required for the conversion of trialkyl borane to an alcohol?
Which compound reacts with propene to form tripropyl borane?
Name the following step from the mechanism of acid catalysed hydration of ethene.
Identify the nucleophile that attacks the carbocation in the second step of acid catalysed hydration of alkenes?