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6 Nov 2019
An answer and an explanation would be appreciated.
4.) The shown reaction can either undergo substitution via an SN1 or SN2 mechanism. What factor can steer it towards the SN1 route? Br H :Nu solvent (A) Strong nucleophile (B) Strong electrophile (C) Good leaving group (D) Polar protic solvent (E) Polar aprotic solvent 5.) What is wrong with the shown elimination (E2) reaction: DBU DMSO (A) DBU is a bad choice of base (B) DMSO is a bad choice of solvent (C) the major product will be a Z-alkene (D) OH is a bad leaving group (E) there is nothing wrong 6.) What will be the major product of the shown reaction: Br HO н он (E) a 1:1 mixture of C and D Show transcribed image text
An answer and an explanation would be appreciated.
4.) The shown reaction can either undergo substitution via an SN1 or SN2 mechanism. What factor can steer it towards the SN1 route? Br H :Nu solvent (A) Strong nucleophile (B) Strong electrophile (C) Good leaving group (D) Polar protic solvent (E) Polar aprotic solvent 5.) What is wrong with the shown elimination (E2) reaction: DBU DMSO (A) DBU is a bad choice of base (B) DMSO is a bad choice of solvent (C) the major product will be a Z-alkene (D) OH is a bad leaving group (E) there is nothing wrong 6.) What will be the major product of the shown reaction: Br HO н он (E) a 1:1 mixture of C and D
Show transcribed image text Hubert KochLv2
6 Nov 2019