7. Circle the one more stable structure in each of the following pairs of molecules or ions: 8. Inspect the following molecules and label each as Z or E isomers if appropriate. 13 Daw ats Br t for the following Br 9. Write a reaction mechanism for the addition of hydrogen bromide to 3-methyl-1-butene. Show the carbocation formation and rearrangement leading to the major 3° alkyl bromide product Gly CH
7. Circle the one more stable structure in each of the following pairs of molecules or ions: 8. Inspect the following molecules and label each as Z or E isomers if appropriate. 13 Daw ats Br t for the following Br 9. Write a reaction mechanism for the addition of hydrogen bromide to 3-methyl-1-butene. Show the carbocation formation and rearrangement leading to the major 3° alkyl bromide product Gly CH
Chemistry
10th Edition
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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7-9 please separate answers
![CHE 231 Organic Chemistry
April 25, 2022
page 2
4. Draw as a polygon structure one of the following steroids:
Estradiol [Estr-1,3,5(10)-triene-3,17B-diol) or
Testosterone 17B-hydroxyandrost-4-ene-3-one
5. Fill in non-bonding electrons and draw the resonance forms using arrows on one structure to show
the movement of electrons in the following ions or molecules.
[a] he
[b]
chair fom of the e
6. Acid base reactions reach equilibrium almost instantly on mixing. Draw the conjugate acid and
conjugate base for the following a proton transfer reactions, and using the pKa values you are given,
circle the arrow in the direction that the equilibrium lies.
[a]
pka =4.7
[b] Ctz Qt zNHz
pka = 10,7
12
Two products for the following mc
7. Circle the one more stable structure in each of the following pairs of molecules or ions:
CHS
it
Cr
(H2
8. Inspect the following molecules and label each as Z or E isomers if appropriate.
13 Daw at3 or
duct for
Br
CH3
34-
9. Write a reaction mechanism for the addition of hydrogen bromide to 3-methyl-1-butene. Show the carbocation
formation and rearrangement leading to the major 3° alkyl bromide product
(6)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe9928f20-3b70-4abf-895b-c48ef51932c1%2F2409bc09-0a38-4b47-9ce1-958682cf91a1%2Fph8hxll_processed.jpeg&w=3840&q=75)
Transcribed Image Text:CHE 231 Organic Chemistry
April 25, 2022
page 2
4. Draw as a polygon structure one of the following steroids:
Estradiol [Estr-1,3,5(10)-triene-3,17B-diol) or
Testosterone 17B-hydroxyandrost-4-ene-3-one
5. Fill in non-bonding electrons and draw the resonance forms using arrows on one structure to show
the movement of electrons in the following ions or molecules.
[a] he
[b]
chair fom of the e
6. Acid base reactions reach equilibrium almost instantly on mixing. Draw the conjugate acid and
conjugate base for the following a proton transfer reactions, and using the pKa values you are given,
circle the arrow in the direction that the equilibrium lies.
[a]
pka =4.7
[b] Ctz Qt zNHz
pka = 10,7
12
Two products for the following mc
7. Circle the one more stable structure in each of the following pairs of molecules or ions:
CHS
it
Cr
(H2
8. Inspect the following molecules and label each as Z or E isomers if appropriate.
13 Daw at3 or
duct for
Br
CH3
34-
9. Write a reaction mechanism for the addition of hydrogen bromide to 3-methyl-1-butene. Show the carbocation
formation and rearrangement leading to the major 3° alkyl bromide product
(6)
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