(Hydrogenation): 3,3-dimethylcyclopentene + H2 – (hydrohalogenation reaction): 2,4-dimethyl-3-hexene + HBr → (hydrohalogenation reaction): Cyclohexene + HCI → (hydration reaction): 2-methylbutene + H20 →

(Hydrogenation): 3,3-dimethylcyclopentene + H2 – (hydrohalogenation reaction): 2,4-dimethyl-3-hexene + HBr → (hydrohalogenation reaction): Cyclohexene + HCI → (hydration reaction): 2-methylbutene + H20 →

General, Organic, and Biological Chemistry

7th Edition

ISBN:9781285853918

Author:H. Stephen Stoker

Publisher:H. Stephen Stoker

Chapter13: Unsaturated Hydrocarbons

Section: Chapter Questions

Problem 13.66EP

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

100%

Match the following reactions with its product.

(Hydrogenation): 3,3-dimethylcyclopentene + H2 –
(hydrohalogenation reaction): 2,4-dimethyl-3-hexene + HBr →
(hydrohalogenation reaction): Cyclohexene + HCI →
(hydration reaction): 2-methylbutene + H20 →

Choices:
4-bromo-2,4-dimethylhexane
1,1-dimethylcyclopentane
CI
Br
H
H
chlorocyclohexane

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