
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:Acid chloride #2: (Z)-3-hexenoyl chloride
P.
opy
aste
ChemDoodle
Acid chloride #3: (Z)-4-hexenoyl chloride
P
opy
aste

Transcribed Image Text:Draw the structure of the following three isomeric acid chlorides with chemical formula C,H,CIO.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• Consider E/Z stereochemistry of alkenes.
• In cases where there is more than one answer, just give one.
Acid chloride #1: (E)-4-hexenoyl chloride
C P
aste
орy
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ChemDoodle
Acid chloride #2: (Z)-3-hexenoyl chloride
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- Complete the following reaction, and answer the questions below: OH (NaoH) a) What s the name of this reaction? b) OH in the above reaction is a base or a nucleophile ?arrow_forward1. Draw structures for the following molecules. 1,5-dihydroxypentan-3-one p-nitrobenzaldehyde (3S)-4-hydroxy-3-methylbutanal 3-phenylcyclohex-2-enonearrow_forward2. Name the following aldehydes using the common system of naming: a) H-とーH b) CHy-C-H c) CH-CH CHO ) C-CH-CH-ごーH c)arrow_forward
- draw the structure of (Z)-4-hexenoyl chloridearrow_forwardName the following CH3CH2 1 CH3CCH₂CHCH3 11 CH3CH2 :N(CH3)2 O4,4-Diethyl-N,N-dimethylpentyl-2-amine O4,4-Diethyl-N,N-dimethylpentane-2-amine 4-Ethyl-4,N,N-trimethylhexane-2-amine 4-Ethyl-4,N,N-trimethylhexyl-2-aminearrow_forwardGive the common names for each of the following ethers ot amines (a) CH3---O--CH2CH2CH2CH3 (b) CH3CH2----O---CH2CH3 (c) CH3CH2--N---CH3 I CH3 (d) CH3CH2----N---CH3 | Harrow_forward
- Provide an IUPAC or common name for these compounds.arrow_forward4. Draw the following compounds: 7-iodo-5-methyl-N-propylnon-2-yn-4-amine: 1-chloro-3-isopropylhex-4-en-2-ol 3-tert-butyl-4-(2-methoxyethyl)cyclopentanolarrow_forwardWhat products are formed when the amine below reacts with HC1? CH,CH,CH,-N- -N-CH,CH,CH-CH,CH;CH, A) CH;CH,CH, NH, + CH,CICH,CH;CH;CH;CH, B) CH,CH,CH,- CH,CH CH,CH,CH,CH, + CI C) CH,CH,CH,-N-CH,CH-CH-CH,CH,CH, H,CI D) CH,CH,CH, N-CH,CH,CH,CHCH,CH, + CI"arrow_forward
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