In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?
(i)
SN1 reaction proceeds via the formation of carbocation. The alkyl halide (I) is 3° while (II) is 2°. Therefore, (I) forms 3° carbocation while (II) forms 2° carbocation. Greater the stability of the carbocation, faster is the rate of SN1 reaction. Since 3° carbocation is more stable than 2° carbocation. (I), i.e. 2-chloro-2-methylpropane, undergoes faster SN1 reaction than (II) i.e., 3-chloropentane.
(ii)
The alkyl halide (I) is 2° while (II) is 1°. 2° carbocation is more stable than 1° carbocation. Therefore, (I), 2-chloroheptane, undergoes faster SN1 reaction than (II), 1-chlorohexane.
In a reaction between A and B, the initial rate of reaction (r0) was measured for different initial concentrations of A and B as given below:
A/ mol L - 1 |
0.20 | 0.20 | 0.40 |
B/ mol L - 1 |
0.30 | 0.10 | 0.05 |
r0/ mol L - 1 s - 1 |
5.07 × 10 - 5 |
5.07 × 10 - 5 |
1.43 × 10 - 4 |
What is the order of the reaction with respect to A and B?
NCERT questions are designed to test your understanding of the concepts and theories discussed in the chapter. Here are some tips to help you answer NCERT questions effectively:
Welcome to the NCERT Solutions for Class 12 Chemistry - Chapter . This page offers a step-by-step solution to the specific question from Excercise 1 , Question 8: In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?....
Comments
Que 10.9?
The heat of formation of water is â260 kJ. How much water is decomposed by 130 kJ of heat ? What answer please
Plz give ans of Q10.9