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17 Nov 2019
Question V,Vi Complete the following reactions by writing structures of major products. CH_3 CH_2 CH_2 CH_2 OH + HBr rightarrow BrCH_2 CH_2 CH_2 CH_2 OH + SOCl_2 (+ pyridine) rightarrow C CH_2 CH_2 CH_2 CH_2 F + Nal rightarrow CH_2 C(CH_2)_2 CH_2 OH + HBr rightarrow Explain why does the carbocation intermediate in the hydrolysis of 2-bromo-3-methylbutane rearrange by way of a hydride shift rather than a methyl shift? Show an efficient synthetic route to synthesize 3-methoxy-3-methylhexane from 3-bromo-3-methylhexane. Show a step by step mechanism of the synthesis by showing an intermediate if there is and using all necessary reagents. Is the product optically active? Explain. Circle the best answer for each of the following questions. Which molecule below are chiral? Only I I and III II and III I, II, and III
Question V,Vi
Complete the following reactions by writing structures of major products. CH_3 CH_2 CH_2 CH_2 OH + HBr rightarrow BrCH_2 CH_2 CH_2 CH_2 OH + SOCl_2 (+ pyridine) rightarrow C CH_2 CH_2 CH_2 CH_2 F + Nal rightarrow CH_2 C(CH_2)_2 CH_2 OH + HBr rightarrow Explain why does the carbocation intermediate in the hydrolysis of 2-bromo-3-methylbutane rearrange by way of a hydride shift rather than a methyl shift? Show an efficient synthetic route to synthesize 3-methoxy-3-methylhexane from 3-bromo-3-methylhexane. Show a step by step mechanism of the synthesis by showing an intermediate if there is and using all necessary reagents. Is the product optically active? Explain. Circle the best answer for each of the following questions. Which molecule below are chiral? Only I I and III II and III I, II, and III
Beverley SmithLv2
27 Jun 2019