Academic Integrity: tutoring, explanations, and feedback — we don’t complete graded work or submit on a student’s behalf.

chanism x / ow v2 Online teaching com/ilmmakeAssignment takeCovalent Activity do

ID: 567194 • Letter: C

Question

chanism x / ow v2 Online teaching com/ilmmakeAssignment takeCovalent Activity do?locator: assignment take&take; AssignmentSessionLocator= assignment take Br KO1-Bu Br 2. a = Proton transfer b: Lewis acid base e = Electrophilic addition f El Elimination g-E2 Elimination hSyl Nucleophilic substitution iSy2 Nucleophilic substitution j Electrophilic aromatic substitution Radical chain substitution d Radical chain addition Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -j for your req answers Submit Answer Retry Entire Group 5 more group attempts remaining Previous

Explanation / Answer

1) g) E2 elimination reaction

Explanation: KOt-Bu is a strong base which gives elimination reaction and produces alkene as product.

2) a) proton transfer

Explanation: LDA is a strong base which abstracts acidic proton and produces carbanion as product.

Hire Me For All Your Tutoring Needs
Integrity-first tutoring: clear explanations, guidance, and feedback.
Drop an Email at
drjack9650@gmail.com
Chat Now And Get Quote