Chemistry: An Atoms-Focused Approach
14th Edition
ISBN: 9780393912340
Author: Thomas R. Gilbert, Rein V. Kirss, Natalie Foster
Publisher: W. W. Norton & Company
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option choice:
Isoleucine
Histidine
Threonine
Alanine
Lysine
Aspartate
Tryptophan
Tyrosine
Leucine
Arginine
Cysteine
Asparagine
Valine
Glutamine
Glycine
Methionine
Serine
Proline
Phenylalanine
Glutamate
sketch the nature of the metal-alkylidene bonding interactions.
Part C
The perspective formula of isoleucine, an amino acid, is provided below.
HOOC
H₂NIC
H
川
CH3
CH,CH3
Draw the Newman projection in staggered conformation for isoleucine by viewing the molecule along the
C-2-C-3 bond.
1. Edit the Newman projection on the canvas.
2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups.
3. If you need to start over, Undo or choose a Newman projection from the Templates toolbar
(bottom).
Important: Never delete the hydrogen atoms or bonds directly attached to the template, and do not move
them by dragging or dropping them. That will break the projections structures. Only replace them!
▸ View Available Hint(s)
0 2
H± 3D
EXP.
L
ד
י
CONT. 2
H
0
N
о
Chapter 1 Solutions
Chemistry: An Atoms-Focused Approach
Ch. 1 - Prob. 1.1VPCh. 1 - Prob. 1.2VPCh. 1 - Prob. 1.3VPCh. 1 - Prob. 1.4VPCh. 1 - Prob. 1.5VPCh. 1 - Prob. 1.6VPCh. 1 - Prob. 1.7QACh. 1 - Prob. 1.8QACh. 1 - Prob. 1.9QACh. 1 - Prob. 1.10QA
Ch. 1 - Prob. 1.11QACh. 1 - Prob. 1.12QACh. 1 - Prob. 1.13QACh. 1 - Prob. 1.14QACh. 1 - Prob. 1.15QACh. 1 - Prob. 1.16QACh. 1 - Prob. 1.17QACh. 1 - Prob. 1.18QACh. 1 - Prob. 1.19QACh. 1 - Prob. 1.20QACh. 1 - Prob. 1.21QACh. 1 - Prob. 1.23QACh. 1 - Prob. 1.24QACh. 1 - Prob. 1.25QACh. 1 - Prob. 1.26QACh. 1 - Prob. 1.27QACh. 1 - Prob. 1.28QACh. 1 - Prob. 1.29QACh. 1 - Prob. 1.30QACh. 1 - Prob. 1.31QACh. 1 - Prob. 1.32QACh. 1 - Prob. 1.33QACh. 1 - Prob. 1.34QACh. 1 - Prob. 1.35QACh. 1 - Prob. 1.36QACh. 1 - Prob. 1.37QACh. 1 - Prob. 1.38QACh. 1 - Prob. 1.39QACh. 1 - Prob. 1.40QACh. 1 - Prob. 1.41QACh. 1 - Prob. 1.42QACh. 1 - Prob. 1.43QACh. 1 - Prob. 1.44QACh. 1 - Prob. 1.45QACh. 1 - Prob. 1.46QACh. 1 - Prob. 1.47QACh. 1 - Prob. 1.48QACh. 1 - Prob. 1.49QACh. 1 - Prob. 1.50QACh. 1 - Prob. 1.51QACh. 1 - Prob. 1.52QACh. 1 - Prob. 1.53QACh. 1 - Prob. 1.54QACh. 1 - Prob. 1.55QACh. 1 - Prob. 1.56QACh. 1 - Prob. 1.57QACh. 1 - Prob. 1.58QACh. 1 - Prob. 1.59QACh. 1 - Prob. 1.60QACh. 1 - Prob. 1.61QACh. 1 - Prob. 1.62QACh. 1 - Prob. 1.63QACh. 1 - Prob. 1.64QACh. 1 - Prob. 1.65QACh. 1 - Prob. 1.66QACh. 1 - Prob. 1.67QACh. 1 - Prob. 1.68QACh. 1 - Prob. 1.69QACh. 1 - Prob. 1.70QACh. 1 - Prob. 1.71QACh. 1 - Prob. 1.72QACh. 1 - Prob. 1.73QACh. 1 - Prob. 1.74QACh. 1 - Prob. 1.75QACh. 1 - Prob. 1.76QACh. 1 - Prob. 1.77QACh. 1 - Prob. 1.78QACh. 1 - Prob. 1.79QACh. 1 - Prob. 1.80QACh. 1 - Prob. 1.81QACh. 1 - Prob. 1.82QACh. 1 - Prob. 1.83QACh. 1 - Prob. 1.84QACh. 1 - Prob. 1.85QACh. 1 - Prob. 1.86QACh. 1 - Prob. 1.87QACh. 1 - Prob. 1.88QACh. 1 - Prob. 1.90QACh. 1 - Prob. 1.91QACh. 1 - Prob. 1.92QACh. 1 - Prob. 1.93QACh. 1 - Prob. 1.94QA
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- Use the literature Ka value of the acetic acid, and the data below to answer these questions. Note: You will not use the experimental titration graphs to answer the questions that follow. Group #1: Buffer pH = 4.35 Group #2: Buffer pH = 4.70 Group #3: Buffer pH = 5.00 Group #4: Buffer pH = 5.30 Use the Henderson-Hasselbalch equation, the buffer pH provided and the literature pKa value of acetic acid to perform the following: a) calculate the ratios of [acetate]/[acetic acid] for each of the 4 groups buffer solutions above. b) using the calculated ratios, which group solution will provide the best optimal buffer (Hint: what [acetate]/[acetic acid] ratio value is expected for an optimal buffer?) c) explain your choicearrow_forwardHow would you prepare 1 liter of a 50 mM Phosphate buffer at pH 7.5 beginning with K3PO4 and 1 M HCl or 1 M NaOH? Please help and show calculations. Thank youarrow_forwardDraw the four most importantcontributing structures of the cation intermediate thatforms in the electrophilic chlorination of phenol,(C6H5OH) to form p-chlorophenol. Put a circle aroundthe best one. Can you please each step and also how you would approach a similar problem. Thank you!arrow_forward
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