188k views
5 votes
1,3-pentadiene and 1,4-pentadiene are compared with respect to their intrinsic stability and reaction with Hl. The correct statement is:

A. 1,3-pentadiene is more stable and more reactive than 1,4-pentadiene
B. 1,3-pentadiene is less stable and less reactive than 1,4-pentadiene
C. 1,3-pentadiene is more stable but less reactive than 1,4-pentadiene
D. 1,3-pentadiene is less stable but more reactive than 1,4-pentadiene

User Alecto
by
7.8k points

1 Answer

4 votes

Final answer:

The correct answer is Option C. 1,3-pentadiene is more stable but less reactive than 1,4-pentadiene.

Step-by-step explanation:

In comparing 1,3-pentadiene and 1,4-pentadiene with respect to their intrinsic stability and reaction with HI, we can consider the concept of delocalization of electrons, which results in a more stable molecule. Based on this, we can conclude that 1,3-pentadiene, which has a conjugated system of double bonds, is more stable than 1,4-pentadiene. However, with regard to reactivity, 1,3-pentadiene is actually less reactive than 1,4-pentadiene due to the delocalization of electrons making it less accessible for reaction.

User Jww
by
8.2k points
Welcome to QAmmunity.org, where you can ask questions and receive answers from other members of our community.