Which reaction is expected to be faster, addition of HBr to cyclohexene or to 1-methylcyclohexene is to be stated. Concept introduction: The addition of hydrogen halides to alkenes takes place through the formation of a more stable carbocation intermediate by the attack of the Ï€ electrons of the double bond on the positively polarized hydrogen of the hydrogen halide. The halogen is eliminated as a halide ion. In the second step, the halide ion reacts with the carbocation to yield the product. To state: Among the two reactions, the addition of HBr to cyclohexene and addition of HBr to 1-merhylcyclohexene which is faster.

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Draw all resonance structures for the following ion: CH₂ Draw all resonance structures on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. 2D ד CONT HD EXP CON ? 1 [1] Α 12 Marvin JS by Chemaxon A DOO H C N Br I UZ OSPF

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Chapter 8.SE, Problem 45AP

Interpretation Introduction

Interpretation:

Which reaction is expected to be faster, addition of HBr to cyclohexene or to 1-methylcyclohexene is to be stated.

Concept introduction:

The addition of hydrogen halides to alkenes takes place through the formation of a more stable carbocation intermediate by the attack of the Ï€ electrons of the double bond on the positively polarized hydrogen of the hydrogen halide. The halogen is eliminated as a halide ion. In the second step, the halide ion reacts with the carbocation to yield the product.

To state:

Among the two reactions, the addition of HBr to cyclohexene and addition of HBr to 1-merhylcyclohexene which is faster.

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