(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 alkene or alkyne yields the following products after oxidative cleavage with ozone? Click the
"draw structure" button to launch the drawing utility.
and two equivalents of CH2=O
draw structure ...
H-Br
Energy
1) Draw the step-by-step mechanism by which 3-methylbut-1-ene is converted into
2-bromo-2-methylbutane.
2) Sketch a reaction coordinate diagram that shows how the internal energy (Y-
axis) of the reacting species change from reactants to intermediate(s) to product.
Br
2. Draw the missing structure(s) in each of the following reactions. The missing
structure(s) can be a starting material or the major reaction product(s).
C5H10
H-CI
CH2Cl2
CI
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