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Haloalkanes and Haloarenes

Tripura Board · Class 12 · Chemistry

Practice quiz for Haloalkanes and Haloarenes — Tripura Board Class 12 Chemistry. MCQs and questions with answers to test your preparation.

29 questions22 flashcards5 concepts

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A flowchart illustrating the general reaction of alcohols with halogen acids (HX) to form alkyl halides, showing the reactivity order of primary, secondary, and tertiary alcohols.
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Quick Quiz: Haloalkanes and Haloarenes

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1

What is the IUPAC name of (CH₃)₃CBr?

2

Which reagent is preferred for converting alcohols to alkyl chlorides?

3

Primary alkyl halides undergo nucleophilic substitution mainly by which mechanism?

4

What is the major product when 2-bromopentane undergoes elimination reaction with alcoholic KOH?

29 Questions·
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Sample Questions

1multiple correct

Which of the following are characteristics of the C-X bond in haloalkanes?

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The bond is polar, Carbon bears partial positive charge, Halogen bears partial negative charge, Bond length increases from C-F to C-I

Halogens are more electronegative than carbon, making the C-X bond polar with carbon having δ+ charge and halogen having δ- charge. As we go down the halogen group, atomic size increases, so bond length increases from C-F (139 pm) to C-I (214 pm).

2multiple correct

Which of the following factors affect the reactivity of haloalkanes in nucleophilic substitution?

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Nature of halogen, Nature of alkyl group, Nature of nucleophile, Temperature

Reactivity depends on: nature of halogen (I > Br > Cl > F), alkyl group structure (3° > 2° > 1° for SN1), nucleophile strength, and temperature. Color has no effect on reactivity.

3multiple choice

Grignard reagents are prepared by reacting alkyl halides with:

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Magnesium in dry ether

Grignard reagents (RMgX) are formed by the reaction of alkyl halides with magnesium metal in dry ether. The reaction must be carried out in anhydrous conditions to prevent reaction with water.

4multiple correct

Why are aryl halides less reactive than alkyl halides towards nucleophilic substitution?

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Resonance stabilization, sp² hybridization of carbon, Instability of phenyl cation, Electron repulsion

Aryl halides are less reactive due to: (1) resonance giving C-X partial double bond character, (2) sp² carbon being more electronegative than sp³, (3) phenyl cation instability ruling out SN1, and (4) electron-rich nucleophile repulsion by electron-rich benzene ring. Molecular weight doesn't affect reactivity.

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What are the important topics in Haloalkanes and Haloarenes for Tripura Board Class 12 Chemistry?
Haloalkanes and Haloarenes covers several key topics that are frequently asked in Tripura Board Class 12 board exams. Focus on the core concepts listed on this page and practise related questions to build confidence.
How to score full marks in Haloalkanes and Haloarenes — Tripura Board Class 12 Chemistry?
Understand the core concepts first, then work through the 29 practice questions available for this chapter. Revise formulas and definitions regularly, and use flashcards for quick recall before the exam.

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