Answer:
See explanation and image attached for details
Explanation:
The reaction involves the heterolytic fission of the Br-Br bond in the bromine molecule to yield a bromine cation which attacks the but-1-ene to form a cyclic intermediate called the brominium ion. The bromine anion must now attack from the opposite face of the brominium ion due to steric clashes to form a product of a 1,2-dibromoalkane having the anti- stereochemistry.
Answer:
2-chloro-1-methyl-cyclohex-1,4-diene.
Explanation:
Hello,
In this case, the addition of hydrochloric acid acts as an electrophilic atack in which the hydrogen bonded to the double-bonded carbon connected to the carbon with the methyl substitution is substituted by the chlorine from the hydrochloric acid, in such a way, 2-chloro-1-methyl-cyclohex-1,4-diene is produced as one equivalent of HCl is used therefore one substitution will be attained for chlorine, and hydrogen as a side product as shown on the attached picture.
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