5. For which reaction mechanisms-SN1, SN2, E1 or E2-are each of the following statements true? A statement may be true for one or more mechanisms. (Write all that apply next to the statement.) I haven't decided whether I will put questions in this type of format, but you still need to know the answers to them. a. The mechanism involves cation intermediates. b. The mechanism has 2 steps. c. The reaction rate increases with better leaving groups.

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5. For which reaction mechanisms-SN1, SN2, E1 or E2-are each of the following statements true?
A statement may be true for one or more mechanisms. (Write all that apply next to the
statement.) I haven't decided whether I will put questions in this type of format, but you still
need to know the answers to them.
a. The mechanism involves cation intermediates.
b. The mechanism has 2 steps.
c.
The reaction rate increases with better leaving groups.
d. The reaction rate increases when the solvent is changed from CH3OH to (CH3)2SO.
e. The reaction rate depends on the concentration of alkyl halide only.
f. The mechanism is concerted.
g. Racemization at a stereogenic center occurs.
h. Tertiary (30) alkyl halides react faster than 2° or 1° alkyl halides.
i. The reaction follows a second-order rate equation..
j. The reaction is stereospecific with 100% inversion at the reaction site.
Transcribed Image Text:5. For which reaction mechanisms-SN1, SN2, E1 or E2-are each of the following statements true? A statement may be true for one or more mechanisms. (Write all that apply next to the statement.) I haven't decided whether I will put questions in this type of format, but you still need to know the answers to them. a. The mechanism involves cation intermediates. b. The mechanism has 2 steps. c. The reaction rate increases with better leaving groups. d. The reaction rate increases when the solvent is changed from CH3OH to (CH3)2SO. e. The reaction rate depends on the concentration of alkyl halide only. f. The mechanism is concerted. g. Racemization at a stereogenic center occurs. h. Tertiary (30) alkyl halides react faster than 2° or 1° alkyl halides. i. The reaction follows a second-order rate equation.. j. The reaction is stereospecific with 100% inversion at the reaction site.
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