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
To give:
The product expected, along with its stereochemistry, when Cl2 is added to 1,2-dimethylcyclohexane.
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Chapter 8 Solutions
Organic Chemistry
- Two substitution products result from the reaction between 3-chloro-3-methyl-1- butene with sodium acetate (CH3COO – Na +) in acetic acid under SN1. Identify the products.arrow_forwardIdentify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.arrow_forwardDraw the organic product obtained by hydroboration-oxidation of each of the following alkenes: (a) trans-2-pentene, (b) 2-tert-butyl-3,3-dimethyl-1- butene, and (c) 1-methylcyclohexene. Having done this, draw the product of the acid-catalyzed hydration of these same alkenes. How do the reaction products differ?arrow_forward
- Write the monobromination products of 1,4-dimethylcyclohexane and calculate the percentages of each product. Which is the major product?arrow_forward1. Reaction of 2,3-dimethyl-1-butene with HBr leads to an alkyl bromide, C6H13Br. On treatment of this alkyl halide with KOH in methanol, elimination of HBr occurs and a hydrocarbon that is isometric with the starting alkene is formed. What is the structure of this hydrocarbon and how do you think it is formed from an alkyl bromide? 2. 1-Octen-3-ol is a potent mosquito attractant commonly used in mosquito traps. A number of reactions, including hydrogenation, will transform 1-Octen-3-ol into a less effective molecule. Write a complete reaction equation for the hydrogenation of this alkenol.arrow_forwardDraw the formulas of the reactants and products of the reaction: 2-ethylbutanoyl bromide with excess ethylmagnesium bromide and heating the product with concentrated H2SO4.arrow_forward
- Name the possible alkenes which will yield 1-chloro-1-methylcyclohexane on their reaction with HCl. Write the reactions involved.arrow_forward2- Give the product for the addition of chlorine when HCl reacts with 3-Hexyne in acetic acid (CH3COOH). Show the correct stereochemistry, (is the product Z or E isomer). Identify the product in the following reaction: CH3CH₂CH₂C=CH + 2Cl₂ 3- What products are obtained by the hydration of the following Alkyne: CH3CH₂CH₂C=CCH₂CH₂CH3 1 ?arrow_forwardName (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.arrow_forward
- Draw the structure of each product from the reaction of benzene with 2-chloro-1-methylcyclohexane using AlCl 3 as the catalyst and Identify the major product.arrow_forward(1) Predict the outcome of the addition of HBr to (a) trans-2-pentene, (b) 2-methyl-2-butene, and (c) 4-methylcyclohexene. How many isomers can be formed in each case? (2) Addition of HBr to 3,3-dimethyl-1-butene gives a mixture of two isomeric alkyl bromide products. Draw structures for the two products, and give a mechanistic explanation for their formation.arrow_forwardHow many alkenes or cycloalkenes with the general formula C9H16 can you treat with HCl to obtain 1-chloro-1-ethyl-3,4-dimethylcyclopentane as a major product?arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning