Which of the following statements is invalid-

Question

Which of the following statements is invalid- (A) the more stable the carbocation the faster it is formed (B) propyl cation changes to more stable isopropyl carbonation by 1,2 shift of a hydrogen (C) isopropyl chloride reacts with sodium ethoxide to form 1- ethoxypropane (D) propyl halides reacts with sodium ethoxide to form 1- ethoxypropane

Tardigrade Admin · Accepted Answer

2° halides have greater tendency for elimination then substitution due to steric hindrance. Thus with C2H5ONa+ give mainly alkene as major product.

Q. Which of the following statements is invalid-

the more stable the carbocation the faster it is formed

propyl cation changes to more stable isopropyl carbonation by $1, 2$ shift of a hydrogen

isopropyl chloride reacts with sodium ethoxide to form $1 -$ ethoxypropane

propyl halides reacts with sodium ethoxide to form $1 -$ ethoxypropane

$2^{\circ}$ halides have greater tendency for elimination then substitution due to steric hindrance. Thus with $C_{2} H_{5} ON a^{+}$ give mainly alkene as major product.

Q. Which of the following statements is invalid-

the more stable the carbocation the faster it is formed

propyl cation changes to more stable isopropyl carbonation by 1,2 shift of a hydrogen

isopropyl chloride reacts with sodium ethoxide to form 1− ethoxypropane

propyl halides reacts with sodium ethoxide to form 1− ethoxypropane

2∘ halides have greater tendency for elimination then substitution due to steric hindrance. Thus with C2​H5​ONa+ give mainly alkene as major product.

propyl cation changes to more stable isopropyl carbonation by $1, 2$ shift of a hydrogen

isopropyl chloride reacts with sodium ethoxide to form $1 -$ ethoxypropane

propyl halides reacts with sodium ethoxide to form $1 -$ ethoxypropane

$2^{\circ}$ halides have greater tendency for elimination then substitution due to steric hindrance. Thus with $C_{2} H_{5} ON a^{+}$ give mainly alkene as major product.