CHEMISTRY:SCI.IN CONTEXT (CL)-PACKAGE
5th Edition
ISBN: 9780393628173
Author: Gilbert
Publisher: NORTON
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Chapter 16, Problem 16.74QP
Interpretation Introduction
Interpretation: The option that corresponds to the metal chloride that has the lowest
Concept introduction: The more is the positive charge on the metal ion, the higher is the acidity of the solution and lower is the
To determine: The option that corresponds to the metal chloride that has the lowest
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3. The explosive decomposition of 2 mole of TNT (2,4,6-trinitrotoluene) is shown below:
Assume the C(s) is soot-basically atomic carbon (although it isn't actually atomic carbon in real life).
2
CH3
H
NO2
NO2
3N2 (g)+7CO (g) + 5H₂O (g) + 7C (s)
H
a. Use bond dissociation energies to calculate how much AU is for this reaction in kJ/mol.
Part I.
Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff:
Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone
and
(3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism
the formation of the products
For
Show the mechanism for these reactions
Chapter 16 Solutions
CHEMISTRY:SCI.IN CONTEXT (CL)-PACKAGE
Ch. 16.2 - Prob. 1PECh. 16.2 - Prob. 2PECh. 16.3 - Prob. 3PECh. 16.3 - Prob. 4PECh. 16.3 - Prob. 5PECh. 16.3 - Prob. 6PECh. 16.3 - Prob. 7PECh. 16.3 - Prob. 8PECh. 16.4 - Prob. 9PECh. 16.4 - Prob. 10PE
Ch. 16.4 - Prob. 11PECh. 16.4 - Prob. 12PECh. 16.5 - Prob. 13PECh. 16.6 - Prob. 14PECh. 16.8 - Prob. 15PECh. 16.8 - Prob. 16PECh. 16.8 - Prob. 17PECh. 16.8 - Prob. 18PECh. 16.8 - Prob. 19PECh. 16 - Prob. 16.1VPCh. 16 - Prob. 16.2VPCh. 16 - Prob. 16.3VPCh. 16 - Prob. 16.4VPCh. 16 - Prob. 16.5VPCh. 16 - Prob. 16.6VPCh. 16 - Prob. 16.7VPCh. 16 - Prob. 16.8VPCh. 16 - Prob. 16.9VPCh. 16 - Prob. 16.10VPCh. 16 - Prob. 16.11QPCh. 16 - Prob. 16.12QPCh. 16 - Prob. 16.13QPCh. 16 - Prob. 16.14QPCh. 16 - Prob. 16.15QPCh. 16 - Prob. 16.16QPCh. 16 - Prob. 16.17QPCh. 16 - Prob. 16.18QPCh. 16 - Prob. 16.19QPCh. 16 - Prob. 16.20QPCh. 16 - Prob. 16.21QPCh. 16 - Prob. 16.22QPCh. 16 - Prob. 16.23QPCh. 16 - Prob. 16.24QPCh. 16 - Prob. 16.25QPCh. 16 - Prob. 16.26QPCh. 16 - Prob. 16.27QPCh. 16 - Prob. 16.28QPCh. 16 - Prob. 16.29QPCh. 16 - Prob. 16.30QPCh. 16 - Prob. 16.31QPCh. 16 - Prob. 16.32QPCh. 16 - Prob. 16.33QPCh. 16 - Prob. 16.34QPCh. 16 - Prob. 16.35QPCh. 16 - Prob. 16.36QPCh. 16 - Prob. 16.37QPCh. 16 - Prob. 16.38QPCh. 16 - Prob. 16.39QPCh. 16 - Prob. 16.40QPCh. 16 - Prob. 16.41QPCh. 16 - Prob. 16.42QPCh. 16 - Prob. 16.43QPCh. 16 - Prob. 16.44QPCh. 16 - Prob. 16.45QPCh. 16 - Prob. 16.46QPCh. 16 - Prob. 16.47QPCh. 16 - Prob. 16.48QPCh. 16 - Prob. 16.49QPCh. 16 - Prob. 16.50QPCh. 16 - Prob. 16.51QPCh. 16 - Prob. 16.52QPCh. 16 - Prob. 16.53QPCh. 16 - Prob. 16.54QPCh. 16 - Prob. 16.55QPCh. 16 - Prob. 16.56QPCh. 16 - Prob. 16.57QPCh. 16 - Prob. 16.58QPCh. 16 - Prob. 16.59QPCh. 16 - Prob. 16.60QPCh. 16 - Prob. 16.61QPCh. 16 - Prob. 16.62QPCh. 16 - Prob. 16.63QPCh. 16 - Prob. 16.64QPCh. 16 - Prob. 16.65QPCh. 16 - Prob. 16.66QPCh. 16 - Prob. 16.67QPCh. 16 - Prob. 16.68QPCh. 16 - Prob. 16.69QPCh. 16 - Prob. 16.70QPCh. 16 - Prob. 16.71QPCh. 16 - Prob. 16.72QPCh. 16 - Prob. 16.73QPCh. 16 - Prob. 16.74QPCh. 16 - Prob. 16.75QPCh. 16 - Prob. 16.76QPCh. 16 - Prob. 16.77QPCh. 16 - Prob. 16.78QPCh. 16 - Prob. 16.79QPCh. 16 - Prob. 16.80QPCh. 16 - Prob. 16.81QPCh. 16 - Prob. 16.82QPCh. 16 - Prob. 16.83QPCh. 16 - Prob. 16.84QPCh. 16 - Prob. 16.85QPCh. 16 - Prob. 16.86QPCh. 16 - Prob. 16.87QPCh. 16 - Prob. 16.88QPCh. 16 - Prob. 16.89QPCh. 16 - Prob. 16.90QPCh. 16 - Prob. 16.91QPCh. 16 - Prob. 16.92QPCh. 16 - Prob. 16.93QPCh. 16 - Prob. 16.94QPCh. 16 - Prob. 16.95QPCh. 16 - Prob. 16.96QPCh. 16 - Prob. 16.97QPCh. 16 - Prob. 16.98QPCh. 16 - Prob. 16.99QPCh. 16 - Prob. 16.100QPCh. 16 - Prob. 16.101QPCh. 16 - Prob. 16.102QPCh. 16 - Prob. 16.103QPCh. 16 - Prob. 16.104QPCh. 16 - Prob. 16.105QPCh. 16 - Prob. 16.106QPCh. 16 - Prob. 16.107QPCh. 16 - Prob. 16.108QPCh. 16 - Prob. 16.109QPCh. 16 - Prob. 16.110QPCh. 16 - Prob. 16.111APCh. 16 - Prob. 16.112APCh. 16 - Prob. 16.113APCh. 16 - Prob. 16.114APCh. 16 - Prob. 16.115APCh. 16 - Prob. 16.116APCh. 16 - Prob. 16.117APCh. 16 - Prob. 16.118AP
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- Draw the stepwise mechanismarrow_forwardDraw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forward
- Draw stepwise mechanismarrow_forwardPart I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: a) Give the major reason for the exposure of benzophenone al isopropyl alcohol (w/acid) to direct sunlight of pina colone Mechanism For b) Pinacol (2,3-dimethy 1, 1-3-butanediol) on treatment w/ acid gives a mixture (3,3-dimethyl-2-butanone) and 2, 3-dimethyl-1,3-butadiene. Give reasonable the formation of the productsarrow_forwardwhat are the Iupac names for each structurearrow_forward
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