- Which member of each pair gives the greater rate of S 2 reaction with KN in acetone? or From each pair, select the compound that undergoes S 1 solvolysis in ethanol more rapidly CI or Br CI Draw a structural formula for the product of each SN1 reaction. CI ã人 S enantiomer +CH3CH2 0H ethanol + CH30H methanol 0 Cl + CH 3 COH acetic aci Br + CH3OH methanol> Page 3 of 5
Propose a synthesis for each compound from a haloalkane and a nucleophile SH Account for these relative rates of solvolysis in acetic acid. (CH3)3CBr Br 12 10 10 10 Limiting yourself to a single 1,2-shift, suggest a structural formula for a more stable carbocation. (b)å¿ Page 4 of 5
+ CH30 Na methanol Cl Nal acetone acetoe R enantiomer + HCOH (f) CH3CHCH 2 CH 3 R enantiomer formic acid (g) CH3CH2 ONa + CH2-CHCH3CI ethanol
Show transcribed image text- Which member of each pair gives the greater rate of S 2 reaction with KN in acetone? or From each pair, select the compound that undergoes S 1 solvolysis in ethanol more rapidly CI or Br CI Draw a structural formula for the product of each SN1 reaction. CI ã人 S enantiomer +CH3CH2 0H ethanol + CH30H methanol 0 Cl + CH 3 COH acetic aci Br + CH3OH methanol> Page 3 of 5 Propose a synthesis for each compound from a haloalkane and a nucleophile SH Account for these relative rates of solvolysis in acetic acid. (CH3)3CBr Br 12 10 10 10 Limiting yourself to a single 1,2-shift, suggest a structural formula for a more stable carbocation. (b)å¿ Page 4 of 5 + CH30 Na methanol Cl Nal acetone acetoe R enantiomer + HCOH (f) CH3CHCH 2 CH 3 R enantiomer formic acid (g) CH3CH2 ONa + CH2-CHCH3CI ethanol