Draw the major product(s) of the reaction of 1-methylcyclohexene with the following reagents, disregarding stereoisomers:
3. HBr
4. HBr/peroxide

Verified step by step guidance

1. Identify the structure of 1-methylcyclohexene. It is a cyclohexene ring with a double bond and a methyl group attached to one of the carbons in the double bond.
2. For reaction 3 (HBr): Recognize that this is a hydrohalogenation reaction. The double bond will react with HBr, and the reaction will proceed via Markovnikov's rule. This means the hydrogen (H) will add to the carbon in the double bond with more hydrogens already attached, and the bromine (Br) will add to the carbon with fewer hydrogens.
3. Draw the intermediate carbocation formed during the reaction with HBr. The more stable carbocation (secondary or tertiary) will form, as carbocation stability influences the reaction pathway.
4. For reaction 4 (HBr/peroxide): Recognize that the presence of peroxide changes the reaction mechanism to a free radical addition. This reaction proceeds via anti-Markovnikov's rule, where the bromine (Br) adds to the carbon in the double bond with more hydrogens, and the hydrogen (H) adds to the carbon with fewer hydrogens.
5. Draw the major product(s) for both reactions, keeping in mind the regioselectivity (Markovnikov for HBr and anti-Markovnikov for HBr/peroxide). Disregard stereoisomers as instructed.

Key Concepts

Electrophilic Addition Reactions

Electrophilic addition reactions involve the addition of an electrophile to a nucleophile, typically across a double bond. In the case of alkenes like 1-methylcyclohexene, the π bond acts as a nucleophile, reacting with electrophiles such as HBr. This process leads to the formation of a more stable carbocation intermediate, which can then react with a nucleophile to form the final product.

Markovnikov's Rule

Markovnikov's Rule states that in the addition of HX (where X is a halogen) to an alkene, the hydrogen atom will attach to the carbon with the greater number of hydrogen atoms already attached. This rule helps predict the major product of the reaction, as it favors the formation of the more stable carbocation, leading to the most substituted alkyl halide as the final product.

Radical Mechanism in Peroxide Reactions

The presence of peroxides in reactions with HBr leads to a radical mechanism, which differs from the typical electrophilic addition. In this case, the reaction proceeds via the formation of bromine radicals that add to the alkene, resulting in anti-Markovnikov products. This mechanism is crucial for understanding how the presence of peroxides alters the regioselectivity of the reaction.