the order of reactivity towards E2 elimination - 1.Chlorocyclohexane 2. 1- Chlorocyclohex-2-ene 3. 1- Chloro1,methylcyclohexane 4.

Open in App

Solution

Suggest Corrections

Similar questions

Q. The correct reactivity order of following C = C /

C \equiv

C bonds towards

B r^{\oplus}

is:

Q. Arrange the reactivity of alcohols in decreasing order for

E_{1}

elimination reaction.
1.

C H_{3} - H O | C H - C H_{3}

C H_{3} - H O | C | C H_{3} H - C H_{3}

C_{6} H_{5} - H O | C | C H_{3} H - C H_{3}

C H_{3} - C H_{2} - C H_{2} O H

Is it that for both E1 and E2 mechanisms order of reactivity is

3^o > 2^o > 1^o carbocation

Q. The decreasing order of reactivity of following compound towards

O H^{-}

ions is:
(I) 3-nitrobromobenzene
(II) 2, 4, 6-trinitrobromobenzene
(III) 4-nitrobromobenzene
(IV) 2, 4-dinitrobromobenzene

The following compounds are given to you:
2- Bromopentane, 2- Bromo - 2 methyl butane, 1- Bromopentane.
(a) Write the compound which is most reactive towards SN2 reaction.
(b) Write the compound which is optically active.
(c) Write the compound which is most reactive towards β- elimination reaction.

Join BYJU'S Learning Program