(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.
Use solubility rules to complete balance molecular equations, and provide total and net ionic equations.
Silver Nitrate and Iron(III) Nitrate
Copper(II) Sulfate and Ammonium Chloride
Copper(II) Sulfate and Magnesium Chloride
NH₄Cl(aq) + MgCl₂(aq) →
NH₄Cl(aq) + Fe(NO₃)₃(aq) →
NH₄Cl(aq) + BaCl₂(aq) →
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