A secondary butyl free radical is more stable than the primary butyl free radical. It is due to the

Arrange the following alcohols in the decreasing order of their boiling points. 1. n-Butyl alcohol 2. sec-Butyl alcohol

(B) the steric effect of the tert-butyl group. The steric hindrance caused by bulky tert-butyl group results in monosubstitution form heavier iodine and trisubstitution of lighter chlorine. (C) the …

Tert-butyl group is named as: 1, 1 ... The common name of the group, (C H 3) 2 C H C H 2 ...

When a hydrogen is removed from butane, butyl group is obtained. Hence, the structure of 3-methylbutyl group is obtained, when one hydrogen atom is removed from 3-methylbutane. i.e. …

211.Iso-butyl bromide reacts with aq. KOH gives 1.iso-butyl alcohol 2.t-butyl alcohol 3.n-butyl alcohol 4.sec-butyl alcohol CORRECT ANS IS 2.

A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following ? <!--td {border: 1px solid #cccccc;}br {mso-data-placement:same-cell;}--> NEET …

In the following reaction, the steric of the tetra-butyl group which is attached to the benzene ring. That is why, the reactivity of compound Z with different halogens under appropriate condition …

butyl is a four- carbon alkyl radical-C4H9, derived from either of the two isomer of butane. The terms primary, secondary , tertiary and quaternary refer to a carbon attached to one, two, …

Click here:point_up_2:to get an answer to your question :writing_hand:the structure of isobutyl group in an organic compound is 3