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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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
Transcribed Image Text:3-amino-N-methylpropanamide

Transcribed Image Text:r. 4-ethyl-2-oxacyclohexanone
s. methanoic anhydride
t. 1-amino-3-hydroxy valeric acid
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- Instructions: DRAW a structure corresponding to each name a. 3-hexanamine b. N-methylpentylamine c. p-nitroaniline d. N-methylpiperidine e. N,N-dimethylethylamine f. 2-aminocyclohexanone g. 1-propylcyclohexanamine h. N-propylanilinearrow_forward2. In the hydrolysis of amide, what is the identity of the leaving group? What are the final product of the reaction?arrow_forward20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat Carrow_forward
- - 17 Give the IUPAC name for the following compound: Br CO₂H A. 3-bromo-5-methylheptanoic acid B. 3-(1-bromoethyl)-4-methylhexanoic acid C. 3-bromo-4-ethylhexanoic acid D. 3-methyl-5-bromoheptanoic acidarrow_forwardAlkylation or acylation of ester ____ followed by hydrolysis and decarboxylation to give substituted acetone derivativesarrow_forward
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