1
answer
0
watching
484
views
11 Nov 2019
Can you explain why the answer is correct? 1-4) Which of the following compounds would be most reactive toward electrophilic substitution? IV utom d)iv 15) Which of the following compounds would be least reactive toward electrophilic substitution? CHO a) I b) II c) Il that duo dematy insid he virg 16) Which of these species is/are proposed as intermediate(s) in the mechanism for the Birch reduction? a) Radical b) Carbanion and auctions are spli+ c) Radical anion Two of these choices. e)All of these choices. 17) What is the correct IUPAC name for the following compound? UPACYWes a)5.5-Dimethyl-2-heptanone 5-Ethyl-5,5-dimethyl-Methyl-2-octanone 5-Ethyl-5-methyl- 2-hexanone 5,5-Dimethyl-2-octanone e) 3,3-Dimethyl-6-heptanone
Can you explain why the answer is correct?
1-4) Which of the following compounds would be most reactive toward electrophilic substitution? IV utom d)iv 15) Which of the following compounds would be least reactive toward electrophilic substitution? CHO a) I b) II c) Il that duo dematy insid he virg 16) Which of these species is/are proposed as intermediate(s) in the mechanism for the Birch reduction? a) Radical b) Carbanion and auctions are spli+ c) Radical anion Two of these choices. e)All of these choices. 17) What is the correct IUPAC name for the following compound? UPACYWes a)5.5-Dimethyl-2-heptanone 5-Ethyl-5,5-dimethyl-Methyl-2-octanone 5-Ethyl-5-methyl- 2-hexanone 5,5-Dimethyl-2-octanone e) 3,3-Dimethyl-6-heptanone
Nestor RutherfordLv2
11 Jan 2019