(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.
What products are formed when the following compounds react with ozone and then with dimethyl sulfide?
Draw the carbonyl products formed when each alcohol is oxidized with K 2Cr 2O 7.
Which alcohols can be prepared as a single product by hydroboration– oxidation of an alkene? Which alcohols can be prepared as a single product by the acid-catalyzed addition of H2O to an alkene?
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