
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 14, Problem 37P
Interpretation Introduction
Interpretation:
The protons of
Concept introduction:
Annulenes have a conjugated electron
If the annulene is anti
If the annulene is aromatic, then the direction of the induced magnetic field is opposite to the direction of applied external magnetic field, and the inner protons are more shielded.
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● Biological Macromolecules
Naming and drawing cyclic monosaccharides
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Give the complete common name, including anomer and stereochemistry labels, of the following molecules. You will find helpful information in the ALEKS
resource.
CH2OH
OH
OH
H
H
I
H
OH
OH
H]
H
CH2OH
H
OH
ẞ-L-sorbose
HOCH2
OH
OH H
HOCH2
H
OH OH
H
OH
H
H
CH2OH
OH
H
H
OH
H
I-
H
OH
H
OH
Explanation
Recheck
W
E
R
%
25
α
B
Y
X
&
5
D
F
G
H
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P
What is the missing reactant in this organic reaction?
+ R -A
HO
IN
+ H₂O
Specifically, in the drawing area below draw the skeletal ("line") structure of R.
If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer
box under the drawing area.
Note for advanced students: you may assume no products other than those shown above are formed.
Explanation
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structure.
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ctclix
ALE X A ALE
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Lab
(195 X
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Question 26 of 39 (4 points) | Question Attempt: 1 of Unlimited
Give the IUPAC name.
2,3-dimethylhexane
Part: 1/2
Part 2 of 2
Draw the skeletal structure of a constitutional isomer of the alkane above that contains a different number of carbons in its longest chain.
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Chapter 14 Solutions
Organic Chemistry - Standalone book
Ch. 14.3 - Prob. 1PCh. 14.3 - Prob. 2PCh. 14.4 - The 1H NMR signal for bromoform (CHBr3) appears at...Ch. 14.5 - identify the most shielded and least shielded...Ch. 14.5 - (a) Assign the chemical shifts 1.6, 2.2, and 4.8...Ch. 14.5 - Assign the chemical shifts 1.1, 1.7, 2.0, and 2.3...Ch. 14.5 - Assign the chemical shifts 1.6, 4.0, 7.5, 8.2, and...Ch. 14.6 - The 300-MHz 1H NMR spectrum of 1,4-dimethylbenzene...Ch. 14.6 - Prob. 9PCh. 14.6 - How many signals would you expect to find in the...
Ch. 14.7 - Describe the appearance of the 1H NMR spectrum of...Ch. 14.8 - Describe the appearance of the 1H NMR spectrum of...Ch. 14.11 - Prob. 13PCh. 14.11 - Prob. 14PCh. 14.12 - Hydrogen bonding between the oxygen of dimethyl...Ch. 14.14 - Prob. 16PCh. 14.15 - The 13C NMR spectrum of 1-bromo-3-chloropropane...Ch. 14.15 - Consider carbons x, y, and z in p-methylanisole....Ch. 14.15 - Prob. 19PCh. 14.16 - To which of the compounds of Problem 14.16 does...Ch. 14.18 - DEPT spectra for a compound with the formula...Ch. 14.20 - Vibrational frequencies are sensitive to isotopic...Ch. 14.21 - Prob. 23PCh. 14.22 - Prob. 24PCh. 14.23 - Prob. 25PCh. 14.23 - Which one of the C5H8 isomers shown has its max at...Ch. 14.24 - Knowing what to look for with respect to isotopic...Ch. 14.24 - The base peak appears at m/z105 for one of the...Ch. 14.24 - Mass spectra of 1-bromo-4-propylbenzene and...Ch. 14.25 - Prob. 30PCh. 14 - Each of the following compounds is characterized...Ch. 14 - Deduce the structure of each of the following...Ch. 14 - From among the isomeric compounds of molecular...Ch. 14 - The H1NMR spectrum of fluorene has signals at 3.8...Ch. 14 - Prob. 35PCh. 14 - H1NMR spectra of four isomeric alcohols with...Ch. 14 - Prob. 37PCh. 14 - We noted in Section 14.13 that an NMR spectrum is...Ch. 14 - Identify each of the C4H10O isomers on the basis...Ch. 14 - A compound (C3H7ClO2) exhibited three peaks in its...Ch. 14 - Label nonequivalent carbons in the following...Ch. 14 - Compounds A and B are isomers of molecular formula...Ch. 14 - C13 NMR spectra for four isomeric alkyl bromides...Ch. 14 - Prob. 44PCh. 14 - Prob. 45PCh. 14 - Identify the C3H5Br isomers on the basis of the...Ch. 14 - Prob. 47PCh. 14 - A compound (C8H10O) has the IR and H1NMR spectra...Ch. 14 - Deduce the structure of a compound having the...Ch. 14 - Figure 14.53 presents IR, H1NMR, C13NMR and mass...Ch. 14 - H1NMR, C13NMR, IR, and mass spectra are shown for...Ch. 14 - 1H NMR and IR spectra for a compound with the...Ch. 14 - FriedelCraftsalkylation of benzene with...Ch. 14 - Prob. 54DSPCh. 14 - Prob. 55DSPCh. 14 - Prob. 56DSPCh. 14 - Prob. 57DSPCh. 14 - Prob. 58DSP
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- Predict the product of this organic reaction: + NH2 HO A P+ H2O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. Click and drag to start drawing a structure. ✓arrow_forward个 Stuc X ctclix ALE X A ALE × A ALE X Lab x (195 × Nut x M Inbx EF 目 → C www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-IgNslkr7j8P3jH-IQ1g8NUi-mObKa_ZLx2twjEhK7mVG6PulJI006NcKTV37JxMpz Chapter 12 HW = Question 27 of 39 (5 points) | Question Attempt: 1 of Unlimited Part: 1/2 Part 2 of 2 Give the IUPAC name. Check 3 50°F Clear ©2025 McGraw Hill L Q Search webp a عالياكarrow_forward个 Stuck x ctc xALE X A ALE × A ALE X Lab x (19: x - G www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-lgNslkr7j8P3jH-1Q1g8NUi-mObka ZLx2twjEhK7mVG6PUUIO06 Chapter 12 HW 三 Question 26 of 39 (4 points) 1 Question Attempt: 1 of Unlimited Answer the following questions about the given alkane. Part: 0 / 2 Part 1 of 2 Give the IUPAC name. Skip Part 2 53°F Clear Check × Q Search hp hp 02arrow_forward
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