Consider the Chapter 41 (Microscale), Acetylsalicylic Acid (Aspirin) (pages 529-532) lab. The carbonyl (C=O) group of acetic anhydride acts as an when it reacts with salicylic acid to form aspirin. electrophile Arrhenius base Arrhenius acid nucleophile

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
Section19.SE: Something Extra
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Consider the Chapter 41 (Microscale), Acetylsalicylic Acid
(Aspirin) (pages 529-532) lab.
The carbonyl (C=O) group of acetic anhydride acts as an
when it reacts with salicylic acid to form
aspirin.
electrophile
Arrhenius base
Arrhenius acid
Ⓒnucleophile
Transcribed Image Text:Consider the Chapter 41 (Microscale), Acetylsalicylic Acid (Aspirin) (pages 529-532) lab. The carbonyl (C=O) group of acetic anhydride acts as an when it reacts with salicylic acid to form aspirin. electrophile Arrhenius base Arrhenius acid Ⓒnucleophile
t
Question 43
Consider the Chapter 39: Wittig reaction: Synthesis of
trans-9-(2-phenylethenyl) anthracene (pages 507-510)
lab.
To form the Wittig reagent, benzyltriphenylphosphonium
chloride is reacted with
NaOH
HCI
Triphenylphosphine
9-Anthraaldehyde
Transcribed Image Text:t Question 43 Consider the Chapter 39: Wittig reaction: Synthesis of trans-9-(2-phenylethenyl) anthracene (pages 507-510) lab. To form the Wittig reagent, benzyltriphenylphosphonium chloride is reacted with NaOH HCI Triphenylphosphine 9-Anthraaldehyde
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