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Draw the product for each of the following SN​2 reactions: (a) (S)-2-Chloropentane and NaSH (b) (R)-3-Iodohexane and NaCl (c) (R)-2-Bromohexane and NaCN (d) 1-Bromoheptane and NaOH

Draw the product for each of the following SN​2 reactions: (a) (S)-2-Chloropentane and NaSH (b) (R)-3-Iodohexane and NaCl (c) (R)-2-Bromohexane and NaCN (d) 1-Bromoheptane and NaOH

The product for each of the followingSN​2reactionsTheSN2 reactionis a nucleophilic substitution process in which a bond is broken and a new one issimultaneously created. The step in the reaction that determines rate involves two reacting species.The substrate is attacked from behind in this reaction by thenucleophile. The angle between the nucleophile and the carbon-leaving group bond as it approaches the chosen substrate is 180o. Through a transition state, the carbon-leaving group bond breaks and the carbon-nucleophile bond forms concurrently.The leaving group is now forced out of the transition state on the other side of the carbon-nucleophile link, resulting in the formation of the necessary product. The product is created by inverting thetetrahedral geometryat the central atom, which is a crucial fact to remember.learn more aboutSN2 reactionhere:brainly.com/question/14080839#SPJ4...

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