Introduction To Chemistry 5th Edition
5th Edition
ISBN: 9781260162097
Author: BAUER
Publisher: MCG
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Chapter 13, Problem 37QP
Interpretation Introduction
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8. Draw all the resonance forms for each of the fling molecules or ions, and indicate the major
contributor in each case, or if they are equivalent (45)
(2)
-PH2
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Also calculate the amount of starting materials chlorobenzaldehyde and p-chloroacetophenone
required to prepare 400 mg of the given chalcone product 1, 3-bis(4-chlorophenyl)prop-2-en-1-one
molar mass ok 1,3-bis(4-Chlorophenyl) prop-2-en-1-one = 277.1591m01
number of moles= 0.400/277.15 = 0.00144 moles
2 x 0.00 144=0.00288 moves
arams of acetophenone = 0.00144 X 120.16 = 0.1739
0.1739x2=0.3469
grams of benzaldehyde = 0.00144X106.12=0.1539
0.1539x2 = 0.3069
Starting materials:
0.3469 Ox acetophenone,
0.3069 of benzaldehyde
3
1.
Answer the questions about the following reaction:
(a) Draw in the arrows that can be used make this reaction occur and draw in the product of substitution in this
reaction. Be sure to include any relevant stereochemistry in the product structure.
+
SK
F
Br
+
(b) In which solvent would this reaction proceed the fastest (Circle one)
Methanol
Acetone
(c) Imagine that you are working for a chemical company and it was your job to perform a similar reaction to the
one above, with the exception of the S atom in this reaction being replaced by an O atom. During the reaction, you
observe the formation of three separate molecules instead of the single molecule obtained above. What is the likeliest
other products that are formed? Draw them in the box provided.
Chapter 13 Solutions
Introduction To Chemistry 5th Edition
Ch. 13 - How do acids and bases differ from other...Ch. 13 - Prob. 2QCCh. 13 - Prob. 3QCCh. 13 - Prob. 4QCCh. 13 - Prob. 5QCCh. 13 - Prob. 6QCCh. 13 - Prob. 1PPCh. 13 - Prob. 2PPCh. 13 - Prob. 3PPCh. 13 - Prob. 4PP
Ch. 13 - Prob. 5PPCh. 13 - Prob. 6PPCh. 13 - Prob. 7PPCh. 13 - Prob. 8PPCh. 13 - Prob. 9PPCh. 13 - Prob. 10PPCh. 13 - Prob. 11PPCh. 13 - Prob. 12PPCh. 13 - Prob. 13PPCh. 13 - Prob. 14PPCh. 13 - Prob. 15PPCh. 13 - Prob. 1QPCh. 13 - Prob. 2QPCh. 13 - Prob. 3QPCh. 13 - Prob. 4QPCh. 13 - Prob. 5QPCh. 13 - Prob. 6QPCh. 13 - Prob. 7QPCh. 13 - Prob. 8QPCh. 13 - Prob. 9QPCh. 13 - Prob. 10QPCh. 13 - Prob. 11QPCh. 13 - Prob. 12QPCh. 13 - Prob. 13QPCh. 13 - Prob. 14QPCh. 13 - Prob. 15QPCh. 13 - Prob. 16QPCh. 13 - Prob. 17QPCh. 13 - Prob. 18QPCh. 13 - Prob. 19QPCh. 13 - Prob. 20QPCh. 13 - Prob. 21QPCh. 13 - Prob. 22QPCh. 13 - Prob. 23QPCh. 13 - Prob. 24QPCh. 13 - Prob. 25QPCh. 13 - Prob. 26QPCh. 13 - How do strong acids and bases differ from weak...Ch. 13 - Prob. 28QPCh. 13 - Prob. 29QPCh. 13 - Prob. 30QPCh. 13 - Prob. 31QPCh. 13 - Prob. 32QPCh. 13 - Prob. 33QPCh. 13 - Prob. 34QPCh. 13 - Prob. 35QPCh. 13 - Prob. 36QPCh. 13 - Prob. 37QPCh. 13 - Prob. 38QPCh. 13 - Sodium fluoride, NaF, and sodium acetate,...Ch. 13 - Prob. 40QPCh. 13 - Prob. 41QPCh. 13 - Prob. 42QPCh. 13 - Prob. 43QPCh. 13 - Prob. 44QPCh. 13 - Prob. 45QPCh. 13 - Prob. 46QPCh. 13 - Prob. 47QPCh. 13 - Prob. 48QPCh. 13 - Prob. 49QPCh. 13 - Prob. 50QPCh. 13 - Prob. 51QPCh. 13 - Prob. 52QPCh. 13 - Prob. 53QPCh. 13 - Prob. 54QPCh. 13 - Prob. 55QPCh. 13 - Prob. 56QPCh. 13 - Prob. 57QPCh. 13 - Prob. 58QPCh. 13 - Prob. 59QPCh. 13 - Prob. 60QPCh. 13 - Prob. 61QPCh. 13 - Prob. 62QPCh. 13 - Prob. 63QPCh. 13 - Prob. 64QPCh. 13 - Prob. 65QPCh. 13 - What is the pH range for acidic solutions? For...Ch. 13 - Prob. 67QPCh. 13 - Prob. 68QPCh. 13 - Prob. 69QPCh. 13 - Prob. 70QPCh. 13 - Prob. 71QPCh. 13 - Prob. 72QPCh. 13 - Prob. 73QPCh. 13 - Prob. 74QPCh. 13 - Prob. 75QPCh. 13 - Prob. 76QPCh. 13 - Prob. 77QPCh. 13 - Prob. 78QPCh. 13 - Prob. 79QPCh. 13 - Prob. 80QPCh. 13 - Prob. 81QPCh. 13 - Prob. 82QPCh. 13 - Prob. 83QPCh. 13 - Prob. 84QPCh. 13 - Prob. 85QPCh. 13 - Prob. 86QPCh. 13 - Prob. 87QPCh. 13 - Prob. 88QPCh. 13 - Prob. 89QPCh. 13 - Prob. 90QPCh. 13 - Prob. 91QPCh. 13 - Prob. 92QPCh. 13 - Prob. 93QPCh. 13 - Prob. 94QPCh. 13 - Prob. 95QPCh. 13 - Prob. 96QPCh. 13 - Prob. 97QPCh. 13 - Prob. 98QPCh. 13 - Prob. 99QPCh. 13 - Prob. 100QPCh. 13 - Prob. 101QPCh. 13 - What would you expect to observe if you ran a...Ch. 13 - Prob. 103QPCh. 13 - Prob. 104QPCh. 13 - Prob. 105QPCh. 13 - Prob. 106QPCh. 13 - Prob. 107QPCh. 13 - Prob. 108QPCh. 13 - Prob. 109QPCh. 13 - Prob. 110QPCh. 13 - Prob. 111QPCh. 13 - Prob. 112QPCh. 13 - Prob. 113QPCh. 13 - Prob. 114QPCh. 13 - Prob. 115QPCh. 13 - Prob. 116QPCh. 13 - Prob. 117QPCh. 13 - Prob. 118QPCh. 13 - Prob. 119QPCh. 13 - Prob. 120QPCh. 13 - Prob. 121QPCh. 13 - Prob. 122QPCh. 13 - Prob. 123QPCh. 13 - Prob. 124QPCh. 13 - Prob. 125QPCh. 13 - Prob. 126QPCh. 13 - Prob. 127QPCh. 13 - Prob. 128QPCh. 13 - Prob. 129QPCh. 13 - What is the pH of a mixture that contains...Ch. 13 - Prob. 131QPCh. 13 - Prob. 132QPCh. 13 - Prob. 133QPCh. 13 - Which of the following weak acids has the anion...Ch. 13 - Prob. 135QPCh. 13 - Prob. 136QPCh. 13 - Prob. 137QPCh. 13 - Prob. 138QPCh. 13 - Prob. 139QPCh. 13 - Prob. 140QPCh. 13 - Prob. 141QPCh. 13 - Prob. 142QPCh. 13 - Prob. 143QPCh. 13 - Prob. 144QPCh. 13 - Prob. 145QPCh. 13 - Prob. 146QPCh. 13 - When 10.0mLofa0.10MHCl solution is diluted to...Ch. 13 - Consider a buffer solution prepared by adding...
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- 3. For the reactions below, draw the arrows corresponding to the transformations and draw in the boxes the reactants or products as indicated. Note: Part A should have arrows drawn going from the reactants to the middle structure and the arrows on the middle structure that would yield the final structure. For part B, you will need to draw in the reactant before being able to draw the arrows corresponding to product formation. A. B. Rearrangement ΘΗarrow_forward2. Draw the arrows required to make the following reactions occur. Please ensure your arrows point from exactly where you want to exactly where you want. If it is unclear from where arrows start or where they end, only partial credit will be given. Note: You may need to draw in lone pairs before drawing the arrows. A. B. H-Br 人 C Θ CI H Cl Θ + Br Oarrow_forward4. For the reactions below, draw the expected product. Be sure to indicate relevant stereochemistry or formal charges in the product structure. a) CI, H e b) H lux ligh Br 'Harrow_forward
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