Question

sth:p Words:59 QUESTION 18 Addition of hydrogen chloride to 3,3-dimethyl-1-butene gives a mixture of two isomeric chlorides. Explain why this is the case, using phrases such as energy of transition state s, hyperconjugation, carbocation stability and shift effects TTT Arial 3 (12pt) T-E-JE- 25 Words:0 Path:p Save All Answers Click Save and Submit to save and submit. Click Save All Answers to save all answers.

Answer 1

4028wer. -- h-cl cha-c - Chechy + CH3 -CH-cph CH3-C- CH = CH₂ CH3 3.3 dimetty II butene Hyći Tertiary, chicoide (major) Secondary chicoide minor) Mechanism.' CH3-C- CH = CH. actly re eltz CH₂ 43 CH-chz म secondary cuobocations Tless stable) CH3 Shikt CH₂ CH3 -C- CH-CH3 Cl3 CH3 CHg-G - CH-CH₂ CH3 secondary alkyl halide c) Trobiony cerobocasions (stable) (less stable CH3 - (- cH-CH₂ Testing alkyl CI CH3 halide (stable) 3.3 dimethyl I surene reacts with Hol to gire] Secondary caobocasion It is less stable the fure CH3 group migrate to foron tesniang caraboccoboo which stable therefore in this read we get two products