The stereoisomers present for the given compound 2-methylcyclohexanol has to be drawn. Concept introduction: Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter. Asymmetric centers are Stereocenter. Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups. The equation for finding Stereoisomers from number of asymmetric centers in compounds is 2 n , in which ‘n’ is the number of asymmetric centers.

Question

1/2 - 51% + » GAY Organic Reactions Assignment /26 Write the type of reaction that is occurring on the line provided then complete the reaction. Only include the major products and any byproducts (e.g. H₂O) but no minor products. Please use either full structural diagrams or the combination method shown in the lesson. Skeletal/line diagrams will not be accepted. H3C 1. 2. CH3 A Acid OH Type of Reaction: NH Type of Reaction: + H₂O Catalyst + HBr 3. Type of Reaction: H3C 4. Type Reaction: 5. H3C CH2 + H2O OH + [0] CH3 Type of Reaction: 6. OH CH3 HO CH3 + Type of Reaction: 7. Type of Reaction: + [H]

Answer 1

Question

Chapter 4.12, Problem 33P

Interpretation Introduction

Interpretation:

The stereoisomers present for the given compound 2-methylcyclohexanol has to be drawn.

Concept introduction:

Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereocenter.

Asymmetric centers are Stereocenter. Asymmetric center is a stereocenter which arises to hydrocarbons if the carbon is bonded to four different groups.

The equation for finding Stereoisomers from number of asymmetric centers in compounds is 2n, in which ‘n’ is the number of asymmetric centers.

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