
Organic Chemistry, Books a la Carte Edition (8th Edition)
8th Edition
ISBN: 9780134074580
Author: Bruice, Paula Yurkanis
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 16.8, Problem 33P
(a)
Interpretation Introduction
Interpretation:
The product for the reaction of cyclopentanone with ethylamine should be determined.
(b)
Interpretation Introduction
Interpretation:
The product for the reaction of cyclopentanone with diethylamine should be determined.
(c)
Interpretation Introduction
Interpretation:
The product for the reaction of acetophenone with hexylamine should be determined.
(d)
Interpretation Introduction
Interpretation:
The product for the reaction of acetophenone with cyclohexylamine should be determined.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
4
W
X
D
de
%
F5
人
:0:
>
F6
1. Fill in the missing information
2.
Na2Cr207
H2SO4, H20
OEt
H₂O+
SOC2
CI
SOCI
C
DELL
OH
480
NEOH
F7
B.
F8
prt sc
home
end
insert
F9
F10
F11
F12
&
*
+
VIX -4.
x
人
3. Fill in the missing information
HCN, NaCN
A.
3
D.
E.
H.
P
H₂O'
B.
W
F.
Chaug Br
H.
NOCHON
H20
H*
左
NC.
OH
(Ph)3P
Nech
MeOH,HCI
OH
G.
Ph
DELL
DOW
Be
a. Draw an arrow pushing mechanism for the following.
OH O
HO.
W
X
J
DELL
OH
H₂O
HO
8. Walmart wil
FS
F6
F7
B
F8
prt sc
home
F9
F10
F11
end
F12
inse
A
&
*
+
Chapter 16 Solutions
Organic Chemistry, Books a la Carte Edition (8th Edition)
Ch. 16.1 - Give two names for each of the following:Ch. 16.1 - Prob. 2PCh. 16.1 - Name the following:Ch. 16.2 - Prob. 4PCh. 16.4 - What products are formed when the following...Ch. 16.4 - We saw on the previous page that...Ch. 16.4 - a. How many stereoisomers are obtained from the...Ch. 16.4 - Prob. 9PCh. 16.4 - Write the mechanism for the reaction of acetyl...Ch. 16.4 - Prob. 11P
Ch. 16.4 - Show how the following compounds can be...Ch. 16.4 - Prob. 13PCh. 16.4 - Prob. 14PCh. 16.4 - In the mechanism for cyanohydrin formation, why is...Ch. 16.4 - Prob. 16PCh. 16.4 - Prob. 17PCh. 16.4 - Show two ways to convert an alkyl halide into a...Ch. 16.5 - Prob. 20PCh. 16.5 - Prob. 21PCh. 16.5 - Prob. 22PCh. 16.5 - Prob. 23PCh. 16.6 - Prob. 24PCh. 16.7 - What reducing agents should be used to obtain the...Ch. 16.7 - Prob. 26PCh. 16.8 - Prob. 27PCh. 16.8 - Prob. 28PCh. 16.8 - Prob. 29PCh. 16.8 - The pKa of protonated acetone is about 7.5. and...Ch. 16.8 - Prob. 31PCh. 16.8 - Prob. 32PCh. 16.8 - Prob. 33PCh. 16.8 - Excess ammonia must be used when a primary amine...Ch. 16.8 - The compounds commonly known as amino acids are...Ch. 16.9 - Hydration of an aldehyde is also catalyzed by...Ch. 16.9 - Which ketone forms the most hydrate in an aqueous...Ch. 16.9 - When trichloroacetaldehyde is dissolved in water,...Ch. 16.9 - Which of the following are a. hermiacetals? b....Ch. 16.9 - Prob. 40PCh. 16.9 - Explain why an acetal can be isolated but most...Ch. 16.10 - Prob. 42PCh. 16.10 - Prob. 43PCh. 16.10 - What products would be formed from the proceedings...Ch. 16.10 - a. In a six-step synthesis, what is the yield of...Ch. 16.10 - Show how each of the following compounds could be...Ch. 16.12 - Prob. 47PCh. 16.13 - Prob. 49PCh. 16.14 - Prob. 50PCh. 16.15 - Prob. 51PCh. 16.16 - Prob. 52PCh. 16 - Draw the structure for each of the following: a....Ch. 16 - Prob. 54PCh. 16 - Prob. 55PCh. 16 - Prob. 56PCh. 16 - a. Show the reagents required to form the primary...Ch. 16 - Prob. 58PCh. 16 - Prob. 59PCh. 16 - Using cyclohexanone as the starting material,...Ch. 16 - Propose a mechanism for each of the following...Ch. 16 - Show how each of the following compounds can be...Ch. 16 - Fill in the boxes:Ch. 16 - Prob. 64PCh. 16 - Identify A through O:Ch. 16 - Prob. 66PCh. 16 - Prob. 67PCh. 16 - Prob. 68PCh. 16 - How many signals would the product of the...Ch. 16 - Prob. 70PCh. 16 - Prob. 71PCh. 16 - Prob. 72PCh. 16 - Prob. 73PCh. 16 - Prob. 74PCh. 16 - Prob. 75PCh. 16 - Prob. 76PCh. 16 - Prob. 77PCh. 16 - Prob. 78PCh. 16 - Draw structure for A-D for each of the following:Ch. 16 - Prob. 80PCh. 16 - a. Propose a mechanism for the following reaction:...Ch. 16 - Prob. 82PCh. 16 - A compound gives the following IR spectrum. Upon...Ch. 16 - How can be following compounds be prepared from...Ch. 16 - Prob. 85PCh. 16 - Prob. 86PCh. 16 - Prob. 87PCh. 16 - In the presence of an acid catalyst, acetaldehyde...Ch. 16 - Prob. 89PCh. 16 - Prob. 90PCh. 16 - Prob. 91PCh. 16 - A compound reacts with methylmagnesium bromide...Ch. 16 - Show how each of the following compounds can be...Ch. 16 - Prob. 94PCh. 16 - The pKa values of the carboxylic acid groups of...Ch. 16 - The Baylis-Hillman reaction is a DABCO...Ch. 16 - Prob. 97PCh. 16 - Prob. 98P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Predict the product of this organic reaction: H+ + HO OH A P+H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there isn't any P because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click and drag to start drawing a structure. X 5arrow_forwardWhich synthesis of a Grignard reagent would fail to occur as written? Why is the correct answer D? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forwardDraw the structure of the major organic product(s) of the reaction. H3C 1. DIBAH, toluene -CH3 + 2. H3O DIBAH = diisobutylaluminum hydride, [(CH3)2CHCH2]2AIHarrow_forward
- Which of the following is not an intermediate of the reaction below? Why is the correct answer C? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forwardWhich of the following is the product of the reaction between acetone, CH3COCH3 and methyl amine, CH3NH2? Why is the correct answer A? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forwardWhat is the product of the reaction shown below? Why is the correct answer D? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forward
- Write the systematic name of each organic molecule: structure name П O ☐ O ☐ Oarrow_forwardThe 13C NMR signal for which of the indicated carbons will occur at the frequency (most deshielded)? Why is the correct answer E? Please explain what is happening. Please include a detailed explanation needed to understand the or question.arrow_forwardWhich of the following reagents best achieves the reaction shown below? Why is the correct answer B? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forward
- What is the product of the following reaction sequence? Why is the correct answer D? Please explain what is happening. Please include a detailed explanation and a drawing of steps needed to understand the reaction or question.arrow_forwardPls help ASAParrow_forwardThe reaction of phenylmagnesium bromide (C6H5MgBr) with propanal (CH3CH2CHO)3 followed by hydrolysis yields. A. 2-phenyl-1-propanol B. 1-phenyl-1propanol C. 3-phenyl-2-propanol D. 3-phenyl-1-propanol Why is the correct answer B? Please explain what is happening. Please include a detailed explanation and/or a drawing of steps needed to understand the reaction or question.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning

Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning