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19 Nov 2019
8. (8 pts.) a) In the box next to each structure below, provide an accurate OUPAC or common) name n the box next to each structure below, provide an accurate (IUPAC or common) name for the compound NH NO Cl b.) In the box to the right of each name below, provide the correct structure for the compound p-Xylene m-bromostyrene 9. (18 pts.) In the box to the right of each question below, provide the letter that corresponds with the best possible answer. i.) Which of the following dienes would not react with a dienophile in a Diels-Alder reaction: e.) Neither (a) nor (c) would react with a dienophile in a Diels-Alder rection ii.) Which of the following will form the most stable cationic intermediate in an SN I reaction? H (Br Br H Br e.) Both (b) and (c) will form equally stable intermediates, more stable than (a) and (d).
8. (8 pts.) a) In the box next to each structure below, provide an accurate OUPAC or common) name n the box next to each structure below, provide an accurate (IUPAC or common) name for the compound NH NO Cl b.) In the box to the right of each name below, provide the correct structure for the compound p-Xylene m-bromostyrene 9. (18 pts.) In the box to the right of each question below, provide the letter that corresponds with the best possible answer. i.) Which of the following dienes would not react with a dienophile in a Diels-Alder reaction: e.) Neither (a) nor (c) would react with a dienophile in a Diels-Alder rection ii.) Which of the following will form the most stable cationic intermediate in an SN I reaction? H (Br Br H Br e.) Both (b) and (c) will form equally stable intermediates, more stable than (a) and (d).
Irving HeathcoteLv2
31 May 2019