(a) Interpretation: The products formed by the treatment of CH 3 CH 2 CH 2 CH 2 OTs with the given reagent are to be drawn. Concept introduction: The strong nucleophile, and 1 ° alkyl tosylate both favors an S N 2 mechanism. The S N 2 mechanism proceeds through backside attack, and results a substitution product.
(a) Interpretation: The products formed by the treatment of CH 3 CH 2 CH 2 CH 2 OTs with the given reagent are to be drawn. Concept introduction: The strong nucleophile, and 1 ° alkyl tosylate both favors an S N 2 mechanism. The S N 2 mechanism proceeds through backside attack, and results a substitution product.
Solution Summary: The author explains that the products formed by the treatment of CH_Text3
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(b)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(c)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(d)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product. However, with strong nucleophilic bulky bases reaction proceeds through an E2 mechanism and yield elimination products.
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