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Chemistry in Context
8th Edition
ISBN: 9780073522975
Author: American Chemical Society
Publisher: McGraw-Hill Education
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Question
Chapter 10, Problem 21Q
Interpretation Introduction
Interpretation:
The term pharmacophore has to be explained.
Concept Introduction:
Pharmacophore: It is specific 3D arrangement of
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Students have asked these similar questions
Can you please explain why the correct answer is molecules 2 and 4? Please provide a detailed explanation as well as the two molecules drawn showing what and where it is conjugated.
Can you please explain why the correct answer is (2E, 4Z, 6Z)-2,4,6-Nonatriene? Please include a detailed explanation and a drawing of the structure, with the corresponding parts of the answer labeled. I'm confused why 6 is Z and why it is Nonatriene.
?
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O Macmillan Learning
Using the data in the table, determine the rate constant of the
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[B] (M)
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reaction and select the appropriate units.
1
0.240
0.350
0.0187
2
0.240
0.700
0.0187
A+2B C+D
3
0.480
0.350
0.0748
k =
Units
Chapter 10 Solutions
Chemistry in Context
Ch. 10.2 - Skill Building Checking on Carbon a. Examine the...Ch. 10.2 - Prob. 10.7YTCh. 10.3 - Skill Building Ester Formation Draw structural...Ch. 10.3 - Prob. 10.10YTCh. 10.4 - Prob. 10.11CTCh. 10.4 - You Decide Supersize My Aspirin A friend who...Ch. 10.5 - Modern methods of drug discovery involve...Ch. 10.5 - Make two lists of drugs for each of the two...Ch. 10.5 - See for yourself the shapes of drug molecules by...Ch. 10.6 - Prob. 10.17YT
Ch. 10.6 - Prob. 10.18CTCh. 10.10 - Prob. 10.24CTCh. 10.10 - Prob. 10.25CTCh. 10.10 - Prob. 10.26YTCh. 10 - Prob. 10.1CTCh. 10 - Prob. 1QCh. 10 - Prob. 2QCh. 10 - Prob. 3QCh. 10 - Write the structural formula and line-angle...Ch. 10 - Prob. 5QCh. 10 - Prob. 6QCh. 10 - Prob. 7QCh. 10 - Prob. 8QCh. 10 - Prob. 9QCh. 10 - Prob. 10QCh. 10 - Prob. 11QCh. 10 - Prob. 12QCh. 10 - Prob. 13QCh. 10 - Prob. 14QCh. 10 - Prob. 15QCh. 10 - Prob. 16QCh. 10 - Prob. 17QCh. 10 - Prob. 18QCh. 10 - Prob. 19QCh. 10 - Prob. 20QCh. 10 - Prob. 21QCh. 10 - Sulfanilamide is the simplest sulfa drug, a type...Ch. 10 - Prob. 23QCh. 10 - Prob. 24QCh. 10 - Prob. 25QCh. 10 - Prob. 26QCh. 10 - Molecules as diverse as cholesterol, sex hormones,...Ch. 10 - The text states that some racemic mixtures contain...Ch. 10 - Draw structural formulas for each of these...Ch. 10 - Prob. 30QCh. 10 - In Your Turn 12.12, you were asked to draw...Ch. 10 - Prob. 32QCh. 10 - Prob. 33QCh. 10 - Prob. 34QCh. 10 - Prob. 35QCh. 10 - Prob. 36QCh. 10 - Prob. 37QCh. 10 - Prob. 38QCh. 10 - Prob. 39QCh. 10 - Prob. 40QCh. 10 - Prob. 41QCh. 10 - Prob. 42QCh. 10 - Dorothy Crowfoot Hodgkin first determined the...Ch. 10 - Prob. 46QCh. 10 - Prob. 47QCh. 10 - Prob. 49QCh. 10 - Prob. 51QCh. 10 - Prob. 52QCh. 10 - Prob. 54QCh. 10 - Prob. 55QCh. 10 - Prob. 56QCh. 10 - Prob. 57QCh. 10 - Prob. 58QCh. 10 - Prob. 59Q
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- Can you please explain why structure 3 is the correct answer? I am having trouble understanding why it is aromatic. Can you also label molecules 1, 2, 4, and 5 with the correct nonaromatic or antiaromatic?arrow_forwardQ1. (a) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH3. Use curved arrows to show the electron movement. (b) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH4*. Use curved arrows to show the electron movement.arrow_forwardCan you please explain why answer 5 (V) is the correct answer?arrow_forward
- Can you please explain why structure 3 is the correct answer? Please give a detailed explanation.arrow_forwardPart VII. The H-NMR of a compound with molecular formula C5 H 10 O2 is given below. Find the following: (a) The no. of protons corresponding to each signal in the spectra (6) Give the structure of the compound and assign the signals to each proton in the compound. a 70.2 Integration Values C5H10O2 b 47.7 C 46.5 d 69.5 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 Chemical Shift (ppm) 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 1.0 0.9 0.8arrow_forwardPart 111. 1 H-NMR spectrum of a compound with integration values in red is given below. Answer the following: (a) write the signals in the 'H-NMR spectrum to the corresponding protons on the structure of the molecule below. (b) Identify the theoretical multiplicities for each proton in the compound. Also give the possible. complex splitting patterns assuming J values are not similar. там Br 22 2 3 6 4 7.2 7.0 6.8 6.6 6.4 6.2 6.0 5.8 5.6 5.4 5.2 5.0 4.8 4.6 4.4 4.2 4.0 3.8 3.6 3.4 3.2 3.0 2.8 2.6 2.4 2.2 2.0 1.8 1.6 1.4 1.2 1.0 0.8 0 Chemical Shift (ppm) ra. Br 2 3 6 6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 1.0 0.9 0.8 Chemical Shift (ppm) 2 2 Br 7.3 7.2 7.1 7.0 6.9 6.7 6.6 6.5 6.4 6.3 6.2 6.1 6.0 Chemical Shift (ppm) 5.9 5.8 5.7 5.5 5.4 5.3 5.2 5.0 4.9arrow_forward
- 1600° 1538°C 1493°C In the diagram, the letter L indicates that it is a liquid. Indicate its components in the upper region where only L is indicated. The iron-iron carbide phase diagram. Temperature (°C) 1400 8 1394°C y+L 1200 2.14 y, Austenite 10000 912°C 800a 0.76 0.022 600 400 (Fe) a, Ferrite Composition (at% C) 15 1147°C a + Fe3C 2 3 Composition (wt% C) L 2500 4.30 2000 y + Fe3C 727°C 1500 Cementite (Fe3C) 1000 4 5 6 6.70 Temperature (°F)arrow_forwardNonearrow_forwardPart II. Given below are the 'H-NMR spectrum at 300 MHz in CDC13 and mass spectrum using electron ionization of compound Brian. The FTIR of the said compound showed a strong peak at 1710 cm"). Determine the following: (a) molecular Formula and Degree of unsaturation of compound Brian (b) Basing on the given H-NMR spectrum tabulate the following (i) chemical shifts (ii) integration, ciii) multiplicity and (iv) interferences made for each signal (c) Draw the structure of compound Brian. ) ΕΙ 43 41 27 71 114 (M+) Hmmm 20 30 40 50 60 70 80 90 100 110 120 1H NMR spectrum 300 MHz in CDCl3 2.0 alle 1.0arrow_forward
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