CHEMISTRY W/WRKBK AND SMARTWORK (LL)
5th Edition
ISBN: 9780393693447
Author: Gilbert
Publisher: NORTON
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Chapter 15, Problem 15.96AP
(a)
Interpretation Introduction
Interpretation: The molecular structure of the sodium salt is to be drawn. Whether an aqueous solution of the salt is acidic or basic is to be explained and the reason for the greater solubility of salt in water is to be stated.
Concept introduction: An
To determine: The molecular structure of the sodium salt of Naproxen.
(b)
Interpretation Introduction
To determine: If an aqueous solution of the salt is acidic or basic.
(c)
Interpretation Introduction
To determine: The reason for the greater solubility of salt in water.
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Give reason(s) for six from the followings [using equations if possible] a. Addition of sodium carbonate to sulfanilic acid in the Methyl Orange preparation. b. What happened if the diazotization reaction gets warmed up by mistake. c. Addition of sodium nitrite in acidified solution in MO preparation through the diazotization d. Using sodium dithionite dihydrate in the second step for Luminol preparation. e. In nitroaniline preparation, addition of the acid mixture (nitric acid and sulfuric acid) to the product of step I. f. What is the main reason of the acylation step in nitroaniline preparation g. Heating under reflux. h. Fusion of an organic compound with sodium.
HAND WRITTEN PLEASE
edict the major products of the following organic reaction:
u
A
+
?
CN
Some important notes:
• Draw the major product, or products, of the reaction in the drawing area below.
• If there aren't any products, because no reaction will take place, check the box below the drawing area instead.
Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers.
Explanation
Check
Click and drag to start drawing a structure.
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© 2025 McGraw Hill LLC. All Rights Reserved. Te
LMUNDARY
Sketch the intermediates for A,B,C & D.
Chapter 15 Solutions
CHEMISTRY W/WRKBK AND SMARTWORK (LL)
Ch. 15.2 - Prob. 1PECh. 15.2 - Prob. 2PECh. 15.2 - Prob. 3PECh. 15.3 - Prob. 4PECh. 15.3 - Prob. 5PECh. 15.3 - Prob. 6PECh. 15.4 - Prob. 7PECh. 15.4 - Prob. 8PECh. 15.5 - Prob. 9PECh. 15.5 - Prob. 10PE
Ch. 15.5 - Prob. 11PECh. 15.5 - Prob. 12PECh. 15.6 - Prob. 13PECh. 15.6 - Prob. 14PECh. 15.7 - Prob. 15PECh. 15.8 - Prob. 16PECh. 15.8 - Prob. 17PECh. 15.8 - Prob. 18PECh. 15 - Prob. 15.1VPCh. 15 - Prob. 15.2VPCh. 15 - Prob. 15.3VPCh. 15 - Prob. 15.4VPCh. 15 - Prob. 15.5VPCh. 15 - Prob. 15.6VPCh. 15 - Prob. 15.7VPCh. 15 - Prob. 15.8VPCh. 15 - Prob. 15.9VPCh. 15 - Prob. 15.10VPCh. 15 - Prob. 15.11QPCh. 15 - Prob. 15.12QPCh. 15 - Prob. 15.13QPCh. 15 - Prob. 15.14QPCh. 15 - Prob. 15.15QPCh. 15 - Prob. 15.16QPCh. 15 - Prob. 15.17QPCh. 15 - Prob. 15.18QPCh. 15 - Prob. 15.19QPCh. 15 - Prob. 15.20QPCh. 15 - Prob. 15.21QPCh. 15 - Prob. 15.22QPCh. 15 - Prob. 15.23QPCh. 15 - Prob. 15.24QPCh. 15 - Prob. 15.25QPCh. 15 - Prob. 15.26QPCh. 15 - Prob. 15.27QPCh. 15 - Prob. 15.28QPCh. 15 - Prob. 15.29QPCh. 15 - Prob. 15.30QPCh. 15 - Prob. 15.31QPCh. 15 - Prob. 15.32QPCh. 15 - Prob. 15.33QPCh. 15 - Prob. 15.34QPCh. 15 - Prob. 15.35QPCh. 15 - Prob. 15.36QPCh. 15 - Prob. 15.37QPCh. 15 - Prob. 15.38QPCh. 15 - Prob. 15.39QPCh. 15 - Prob. 15.40QPCh. 15 - Prob. 15.41QPCh. 15 - Prob. 15.42QPCh. 15 - Prob. 15.43QPCh. 15 - Prob. 15.44QPCh. 15 - Prob. 15.45QPCh. 15 - Prob. 15.46QPCh. 15 - Prob. 15.47QPCh. 15 - Prob. 15.48QPCh. 15 - Prob. 15.49QPCh. 15 - Prob. 15.50QPCh. 15 - Prob. 15.51QPCh. 15 - Prob. 15.52QPCh. 15 - Prob. 15.53QPCh. 15 - Prob. 15.54QPCh. 15 - Prob. 15.55QPCh. 15 - Prob. 15.56QPCh. 15 - Prob. 15.57QPCh. 15 - Prob. 15.58QPCh. 15 - Prob. 15.59QPCh. 15 - Prob. 15.60QPCh. 15 - Prob. 15.61QPCh. 15 - Prob. 15.62QPCh. 15 - Prob. 15.63QPCh. 15 - Prob. 15.64QPCh. 15 - Prob. 15.65QPCh. 15 - Prob. 15.66QPCh. 15 - Prob. 15.67QPCh. 15 - Prob. 15.68QPCh. 15 - Prob. 15.69QPCh. 15 - Prob. 15.70QPCh. 15 - Prob. 15.71QPCh. 15 - Prob. 15.72QPCh. 15 - Prob. 15.73QPCh. 15 - Prob. 15.74QPCh. 15 - Prob. 15.75QPCh. 15 - Prob. 15.76QPCh. 15 - Prob. 15.77QPCh. 15 - Prob. 15.78QPCh. 15 - Prob. 15.79QPCh. 15 - Prob. 15.80QPCh. 15 - Prob. 15.81QPCh. 15 - Prob. 15.82QPCh. 15 - Prob. 15.83QPCh. 15 - Prob. 15.84QPCh. 15 - Prob. 15.85QPCh. 15 - Prob. 15.86QPCh. 15 - Prob. 15.87APCh. 15 - Prob. 15.88APCh. 15 - Prob. 15.89APCh. 15 - Prob. 15.90APCh. 15 - Prob. 15.91APCh. 15 - Prob. 15.92APCh. 15 - Prob. 15.93APCh. 15 - Prob. 15.94APCh. 15 - Prob. 15.95APCh. 15 - Prob. 15.96APCh. 15 - Prob. 15.97APCh. 15 - Prob. 15.98APCh. 15 - Prob. 15.99APCh. 15 - Prob. 15.100AP
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- Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? O ? A . If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. . If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. ㅇ 80 F5 F6 A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cente FIGarrow_forwardIn methyl orange preparation, if the reaction started with 0.5 mole of sulfanilic acid to form the diazonium salt of this compound and then it converted to methyl orange [0.2 mole]. If the efficiency of the second step was 50%, Calculate: A. Equation(s) of Methyl Orange synthesis: Diazotization and coupling reactions. B. How much diazonium salt was formed in this reaction? C. The efficiency percentage of the diazotization reaction D. Efficiency percentage of the whole reaction.arrow_forwardHand written equations pleasearrow_forward
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