Give mechanism of this reaction.

How do carbonyl compounds react with HCN. Give mechanism of the reaction.

when 3-methylbutan-2-ol is treated with HBr, the following reaction takes place: Give the mechanism of this reaction. Hint : The secondary carbocation formed in step II rearranges to a more stable tetriary carbocation by a hydride ion shift form the third carbon atom.

when 3-methylbutan-2-ol is treated with HBr, the following reaction takes place: Give the mechanism of this reaction. Hint : The secondary carbocation formed in step II rearranges to a more stable tetriary carbocation by a hydride ion shift form the third carbon atom.

When 3-methylbutan-2-ol is treated with HBr,the, following reaction takes place: Give a mechanism for this reaction. (Hint: The secondary carbocation formed in step If, the arranges to a more stable- tertiary carbocation by a hydride ion shift from 3rd carbon atom.)

Alkanes are monochlorinate with t-butyl hypochlorite as a radical intiator. Give the mechanism of the reaction.

Alkanes are monochlorinate with t-butyl hypochlorite as a radical intiator. Give the mechanism of the reaction.

Give the mechanism of the reaction : C_2H_4+Br_2toBrCH_2CH_2Br

An alkyl halide is reduced to the corresponding alkane by tributyl stannane (C_(4)H_(9))_(3) SnH and by a free radical menchanism in the presence of an initiator, an azo compound that breaks down to N_(2) and a radical. Give the mechanism of the reaction.

An alkyl halide is reduced to the corresponding alkane by tributyl stannane (C_(4)H_(9))_(3) SnH and by a free radical menchanism in the presence of an initiator, an azo compound that breaks down to N_(2) and a radical. Give the mechanism of the reaction.