The product expected, along with its stereochemistry, from the addition of Cl 2 to 1,2-dimethylcyclohexane is to be given. Concept introduction: The reaction of halogens to alkenes occurs with anti stereochemistry, that is, the two halogen atoms come from opposite faces of the double bond- one from top face and other from bottom face. In the first step the addition of halogen to the double bond in the alkenes results in the formation of a cyclic halonium ion with the simultaneous elimination of a halide ion. The larger halonium ion shields one side of the molecule. Hence the attack of the halide ion occurs from the opposite, unshielded side to yield the trans - product. To give: The product expected, along with its stereochemistry, when Cl 2 is added to 1,2-dimethylcyclohexane.

Question

Place the following characteristics into the box for the correct ion. Note that some of the characteristics will not be placed in either bin. Use your periodic table for assistance. Link to Periodic Table Drag the characteristics to their respective bins. ▸ View Available Hint(s) This anion could form a neutral compound by forming an ionic bond with one Ca²+. Reset Help This ion forms ionic bonds with nonmetals. This ion has a 1- charge. This is a polyatomic ion. The neutral atom from which this ion is formed is a metal. The atom from which this ion is formed gains an electron to become an ion. The atom from which this ion is formed loses an electron to become an ion. This ion has a total of 18 electrons. This ion has a total of 36 electrons. This ion has covalent bonds and a net 2- charge. This ion has a 1+ charge. Potassium ion Bromide ion Sulfate ion

Answer 1

Question

Chapter 8.2, Problem 3P

Interpretation Introduction

Interpretation:

The product expected, along with its stereochemistry, from the addition of Cl₂ to 1,2-dimethylcyclohexane is to be given.

Concept introduction:

The reaction of halogens to alkenes occurs with anti stereochemistry, that is, the two halogen atoms come from opposite faces of the double bond- one from top face and other from bottom face. In the first step the addition of halogen to the double bond in the alkenes results in the formation of a cyclic halonium ion with the simultaneous elimination of a halide ion. The larger halonium ion shields one side of the molecule. Hence the attack of the halide ion occurs from the opposite, unshielded side to yield the trans-product.

To give:

The product expected, along with its stereochemistry, when Cl₂ is added to 1,2-dimethylcyclohexane.

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