During the heterolytic cleavage of a carbon-chlorine bond in an alkyl halide like , what are the spe — GOC and Organic Chemistry Basics Chemistry Question
Question
During the heterolytic cleavage of a carbon-chlorine bond in an alkyl halide like $CH_3CH_2-Cl$, what are the specific reaction intermediates produced?
Answer: C
💡 Solution & Explanation
Heterolytic fission of a covalent bond involves the unequal distribution of electrons. Because chlorine is more electronegative than carbon, both bonding electrons move to chlorine, forming an ethyl carbocation ($CH_3CH_2^+$) and a chloride anion ($Cl^-$).
💬Ask on WhatsApp →
Still have doubts about this question?
Send it to our AI chemistry tutor on WhatsApp — gets answered in minutes