Each heterolysis step on the left does not readily occur, but the corresponding one on the right does. Explain why. Hint: Draw the products of each heterolysis and determine the contributions to their driving force. (a) Br Br CH,CHOH CH;CH,OH (b) CH CHOH ? CH;CH,OH (c) you Br Br DMSO CH,CH,OH (d) CHCH,OH ? CH;CH,OH

Please don't use hend raiting

Please show the mechanism with arrow formalism.

Draw and explain this mechanism of the reaction

Draw a representation of the transition state for the following endergonic mechanistic step. H;C-CH=CH, H-OH2 H3C-CH-CH; H,0

Give the product (b) of the synthesis shown.

What would be the major product of this reaction? Click on a letter A through D to answer. CH:CHCHCH2CI AICL CH,CH,CH,CH, CH:CHCHzCH3 C(CH,) CHCH(CHa в

could you propose a mechanism?

In each reaction box, place the best reagent and conditions from the list provided. 1) Br 2) 3) 4) DEET (the active ingredient in over the counter insect repellant) 5) Answer Bank Mg, Et,0 HN(CH, CH, ), (1 equiv.) H,O* CH,COOH CH,CH,NH, CH,CH, Br NH(CH,CH,),(2 cquiv.) НСООСH, H,CO НСООН CH, CH, OH NaCN NaNH, Br,, FeBr, SOCI, CO,

6-46 Show how each compound might be synthesized by the SN2 displacement of an alkyl halide. SCH,CH, (a) -CH₂OH (c) (d) CHÍNH, 6-47 (a) Give twn synthecac fox (CI) qu (b) (e) H₂C=CH-CH₂CN n OLL BU (1) H-C=C-CH₂CH₂CH₂