QUESTION 2 The preparation of a Wittig salt from an alky halide and triphenylphosphine proceeds by a(n). O A. E2 O B. Sn2 O C. E1 O D. free radical O E. Sn1 mechanism. QUESTION 3 Which resonance structure is more reactive as a nucleophile? Ph O A. 1 O B.2 OC both are equally reactive

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter20: Acidity And Pka Of Phenols
Section: Chapter Questions
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QUESTION 2
The preparation of a Wittig salt from an alky halide and triphenylphosphine proceeds by a(n)
O A. E2
O B. Sn2
OC. E1
O D. free radical
O E. Sn1
mechanism.
QUESTION 3
Which resonance structure is more reactive as a nucleophile?
Ph
Ph
O A. 1
O B. 2
OC. both are equally reactive
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F10
F1
F2
F3
F4
F5
F6
23
2
3
4.
7
8
W
Y UI
Transcribed Image Text:QUESTION 2 The preparation of a Wittig salt from an alky halide and triphenylphosphine proceeds by a(n) O A. E2 O B. Sn2 OC. E1 O D. free radical O E. Sn1 mechanism. QUESTION 3 Which resonance structure is more reactive as a nucleophile? Ph Ph O A. 1 O B. 2 OC. both are equally reactive Click Save and Submit to save and submit. Click Save All Answers to save all answers. o search F10 F1 F2 F3 F4 F5 F6 23 2 3 4. 7 8 W Y UI
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