(5) hot acidic KMnO₂ 1 mol HBr C=C-CH₂CH₂ CH₂CH₂-CECH (6) intermediate H.SO, Hg50, H₂. Pd Ba50, (9) enol OH (8) (7) 1,4-addition product (10) keto

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Answer numbers 5 to 10. Thanks!

B.
(5)
Draw the structure of the missing reactant, reaction intermediate, or organic product/s. Use
stereochemical projections only when applicable. Show proper geometry around sp' and sp carbons.
H CH,
CH₂
ㅅ
CH₂CH₂
hot acidic KMnO₂
diluto H₂50,
1 mol HBr
CH₂CH₂-CECH
CI., H.O
MCPBA
-C=C-CH₂CH,
H.SO,
Hp50,
(6)
intermediate
[
(1) + (2) (re-arranged product)
(3)
(4)
H₂. Pd
Ba50,
(9)
enol
OH
(8)
1 –
(7)
1,4-addition product
(10)
keto
Transcribed Image Text:B. (5) Draw the structure of the missing reactant, reaction intermediate, or organic product/s. Use stereochemical projections only when applicable. Show proper geometry around sp' and sp carbons. H CH, CH₂ ㅅ CH₂CH₂ hot acidic KMnO₂ diluto H₂50, 1 mol HBr CH₂CH₂-CECH CI., H.O MCPBA -C=C-CH₂CH, H.SO, Hp50, (6) intermediate [ (1) + (2) (re-arranged product) (3) (4) H₂. Pd Ba50, (9) enol OH (8) 1 – (7) 1,4-addition product (10) keto
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