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Read MoreWelcome to the NCERT Solutions for Class 12 Chemistry - Chapter Haloalkanes and Haloarenes. This page offers a step-by-step solution to the specific question from Exercise 2, Question 10: . With detailed answers and explanations for each chapter, students can strengthen their understanding and prepare confidently for exams. Ideal for CBSE and other board students, this resource will simplify your study experience.
Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:
(i) 1-Bromo-1-methylcyclohexane
(ii) 2-Chloro-2-methylbutane
(iii) 2,2,3-Trimethyl-3-bromopentane.

Saytzeff's rule implies that in dehydrohalogenation reactions, the alkene having a greater number of alkyl groups attached to a doubly bonded carbon atoms is preferably produced. Therefore, alkene (I) i.e., 2-methylbut-2-ene is the major product in this reaction.
(iii)

2,2,3-Trimethyl-3-bromopentane
In the given compound, there are two different sets of equivalent β-hydrogen atoms labelled as a and b. Thus, dehydrohalogenation of the compound yields two alkenes.

According to Saytzeff's rule, in dehydrohalogenation reactions, the alkene having a greater number of alkyl groups attached to the doubly bonded carbon atom is preferably formed. Hence, alkene (I) i.e., 3,4,4-trimethylpent-2-ene is the major product in this reaction.
The reaction between A and B is first order with respect to A and zero order with respect to B. Fill in the blanks in the following table:
| Experiment |
A/ mol L - 1 |
B/ mol L - 1 |
Initial rate/mol L - 1 min - 1 |
| I | 0.1 | 0.1 |
2.0 × 10 - 2 |
| II | -- | 0.2 |
4.0 × 10 - 2 |
| III | 0.4 | 0.4 | -- |
| IV | -- | 0.2 |
2.0 × 10 - 2 |
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Welcome to the NCERT Solutions for Class 12 Chemistry - Chapter . This page offers a step-by-step solution to the specific question from Excercise 2 , Question 10: Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with so....
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