Organic Chemistry Study Guide and Solutions
6th Edition
ISBN: 9781936221868
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Question
Chapter 16, Problem 16.64AP
Interpretation Introduction
Interpretation:
The reason as to why anisole protonates on oxygen in concentrated
Concept introduction:
Electron donating groups substituted on the
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Which is the stronger base: N-methylaniline (C6H5NHCH3) or benzylamine (C6H5CH2NH2). Explain your reasoning, supporting it with appropriate resonance contributors.
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H3O+
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(i) Draw the dissociation reaction for a carboxylic acid in water and define the Ka for this reaction. Write the equation that relates pKa to Ka.
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Chapter 16 Solutions
Organic Chemistry Study Guide and Solutions
Ch. 16 - Prob. 16.1PCh. 16 - Prob. 16.2PCh. 16 - Prob. 16.3PCh. 16 - Prob. 16.4PCh. 16 - Prob. 16.5PCh. 16 - Prob. 16.6PCh. 16 - Prob. 16.7PCh. 16 - Prob. 16.8PCh. 16 - Prob. 16.9PCh. 16 - Prob. 16.10P
Ch. 16 - Prob. 16.11PCh. 16 - Prob. 16.12PCh. 16 - Prob. 16.13PCh. 16 - Prob. 16.14PCh. 16 - Prob. 16.15PCh. 16 - Prob. 16.16PCh. 16 - Prob. 16.17PCh. 16 - Prob. 16.18PCh. 16 - Prob. 16.19PCh. 16 - Prob. 16.20PCh. 16 - Prob. 16.21PCh. 16 - Prob. 16.22PCh. 16 - Prob. 16.23PCh. 16 - Prob. 16.24PCh. 16 - Prob. 16.25PCh. 16 - Prob. 16.26PCh. 16 - Prob. 16.27PCh. 16 - Prob. 16.28PCh. 16 - Prob. 16.29PCh. 16 - Prob. 16.30PCh. 16 - Prob. 16.31PCh. 16 - Prob. 16.32PCh. 16 - Prob. 16.33PCh. 16 - Prob. 16.34PCh. 16 - Prob. 16.35APCh. 16 - Prob. 16.36APCh. 16 - Prob. 16.37APCh. 16 - Prob. 16.38APCh. 16 - Prob. 16.39APCh. 16 - Prob. 16.40APCh. 16 - Prob. 16.41APCh. 16 - Prob. 16.42APCh. 16 - Prob. 16.43APCh. 16 - Prob. 16.44APCh. 16 - Prob. 16.45APCh. 16 - Prob. 16.46APCh. 16 - Prob. 16.47APCh. 16 - Prob. 16.48APCh. 16 - Prob. 16.49APCh. 16 - Prob. 16.50APCh. 16 - Prob. 16.51APCh. 16 - Prob. 16.52APCh. 16 - Prob. 16.53APCh. 16 - Prob. 16.54APCh. 16 - Prob. 16.55APCh. 16 - Prob. 16.56APCh. 16 - Prob. 16.57APCh. 16 - Prob. 16.58APCh. 16 - Prob. 16.59APCh. 16 - Prob. 16.60APCh. 16 - Prob. 16.61APCh. 16 - Prob. 16.62APCh. 16 - Prob. 16.63APCh. 16 - Prob. 16.64APCh. 16 - Prob. 16.65APCh. 16 - Prob. 16.66APCh. 16 - Prob. 16.67APCh. 16 - Prob. 16.68AP
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- Can you answer both please, thank you!arrow_forwardRank the following compounds in terms of increasing acidity of the most acidic proton. Assume all conjugated atoms are coplanar.arrow_forwardQ2Show why the OH functional group, of phenol below, is ortho directing using curly arrows to show the formation of each of the four resonance structures A, B, C and D. Draw all the resonance structures A through D and explain why one resonance structure is more favourable than the other three in directing the electrophile (E*) ortho to the OH functional group.arrow_forward3. Give the pK₂ values for the following compounds and then rank them in terms of increasing acidity. Explain why the values change so dramatically (each pk- unit is an order of magnitude) from one member of the series to the next. H₂C=CH2 H₂C-CH₂ HC=CHarrow_forwardb) 4. Rank the indicated protons in each of the given structures in order of decreasing acidity. Show the details for how you arrived at the answer. SHa HbN & OHCarrow_forwardHydroxylamine, H2NOH, has both an OH functional group and an NH2 functional group, so it can feasibly undergo reaction with a ketone or an aldehyde to produce either an acetal or an imine-like compound called an oxime. (a) Draw each of these mechanisms for the reaction of hydroxylamine with acetone. (b) Which is the major product? Hint: Which step decides the outcome?arrow_forwardXVI. Which of the two nitrogens (a or b) would be more basic (stronger base)? CONCISELY explain why. H ·N· of aarrow_forwardHello, can I get help on this please? I am confused and do not understand! Thank you!arrow_forwardAmides are weak nucleophiles but their conjugate bases are string nucleophiles. The amide drawn below can be deprotonated in four possible locations, labeled A-D but two are considerably more acidic than the others. Draw the two different Bronsted Lowery acid/base reactions (using HO- as the BL base) showing the deprotonation at these two locations. Draw all RS with arrows for both conjugate bases but no hybrids. Based on your resonance analysis which location is the most acidic in the molecule? Why is it most acidic? Amides can also be protonated by a strong acid in two different locations. Draw two different conjugate acids for the amide above as well as RS with arrows for each. Based on your resonance analysis which atom is the most basic in an amide?arrow_forwardkindly answer both and provide some brief explanation. just also want to clarify some difference on item 2. thank youarrow_forwardGive me a clear handwritten answer with explanationarrow_forwardPhenol (hydroxybenzene) behaves as a weak acid. a) Write out the equilibrium equation for its partial dissociation in water. b) Write out the expression for the acid dissociation constant, Ka. d) Draw the conjugate base of phenol and show how it is stabilised by resonance. e) Compare and explain the acidity of phenol (p = 9.9) with that of: cyclohexanol (pk = 16.0) 3-fluorophenol (pK₁ = 9.3) 4-acetylphenol (pK, = 8.1)arrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
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