Pearson eText Fundamentals of General, Organic, and Biological Chemistry -- Instant Access (Pearson+)
8th Edition
ISBN: 9780135213759
Author: John McMurry, David Ballantine
Publisher: PEARSON+
expand_more
expand_more
format_list_bulleted
Question
Chapter 16.6, Problem 16.21P
Interpretation Introduction
Interpretation:
The structure of benzylamine hydrochloride should be written in two different ways, and naming the hydrochloride as an ammonium salt has to be done.
Concept introduction:
Ammonia is very soluble in water giving an alkaline solution which can be neutralized by acids to produce ammonium salts.
In chemistry Structure is the arrangement of
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Draw the structures of the following compounds. (Includes both new and old names.) 3-cyclopentylhexan-3-ol
Salol, the phenyl ester of salicylic acid, is used as an intestinal antiseptic. Draw the structure of phenyl salicylate.
Salicylic acid (o-hydroxybenzoic acid) is used as starting material to prepare aspirin. Draw the structure of salicylic acid.
Chapter 16 Solutions
Pearson eText Fundamentals of General, Organic, and Biological Chemistry -- Instant Access (Pearson+)
Ch. 16.2 - Identify the following compounds as primary,...Ch. 16.2 - Prob. 16.2PCh. 16.2 - Prob. 16.3PCh. 16.2 - Prob. 16.4PCh. 16.2 - Prob. 16.5KCPCh. 16.2 - Prob. 16.6KCPCh. 16.3 - Arrange the following compounds in order of...Ch. 16.3 - Draw the structures of (a) ethylamine and (b)...Ch. 16.4 - Provide compounds that fit the following...Ch. 16.4 - Prob. 16.10P
Ch. 16.4 - Prob. 16.11PCh. 16.5 - Write an equation for the acid-base equilibrium...Ch. 16.5 - Prob. 16.13PCh. 16.5 - Prob. 16.14PCh. 16.5 - Prob. 16.15PCh. 16.5 - Prob. 16.16PCh. 16.6 - Prob. 16.17PCh. 16.6 - Prob. 16.18PCh. 16.6 - Prob. 16.19PCh. 16.6 - Prob. 16.20PCh. 16.6 - Prob. 16.21PCh. 16.6 - Prob. 16.22PCh. 16.7 - Prob. 16.1CIAPCh. 16.7 - Prob. 16.2CIAPCh. 16.7 - Prob. 16.3CIAPCh. 16 - (a) For the compound above, identify each nitrogen...Ch. 16 - The structure of the amino acid lysine (in its...Ch. 16 - Prob. 16.25UKCCh. 16 - Prob. 16.26UKCCh. 16 - Prob. 16.27UKCCh. 16 - Complete the following equations: (a) (b)...Ch. 16 - Prob. 16.29APCh. 16 - Draw the structures corresponding to the following...Ch. 16 - Name the following amines, and classify them as...Ch. 16 - Name the following amines, and identify them as...Ch. 16 - Prob. 16.33APCh. 16 - Which is a stronger base, diethyl ether or...Ch. 16 - Prob. 16.35APCh. 16 - Prob. 16.36APCh. 16 - The compound lidocaine is used medically as a...Ch. 16 - Prob. 16.38APCh. 16 - Draw the structures of the ammonium ions formed...Ch. 16 - Prob. 16.40APCh. 16 - Prob. 16.41APCh. 16 - Prob. 16.42APCh. 16 - Prob. 16.43APCh. 16 - Prob. 16.44APCh. 16 - Prob. 16.45CPCh. 16 - Prob. 16.46CPCh. 16 - Prob. 16.47CPCh. 16 - Prob. 16.48CPCh. 16 - How do amines differ from analogous alcohols in...Ch. 16 - Name at least two undesirable characteristics are...Ch. 16 - Prob. 16.52CPCh. 16 - Complete the following equations (Hint: Answers...Ch. 16 - Prob. 16.54CPCh. 16 - Prob. 16.55CPCh. 16 - Why is cyclohexylamine not considered to be a...Ch. 16 - Prob. 16.57CPCh. 16 - Prob. 16.58GPCh. 16 - 1-Propylamine, 1-propanol, acetic acid, and butane...Ch. 16 - Prob. 16.60GPCh. 16 - Lemon juice, which contains citric acid, is...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.Similar questions
- Drawn are four isomeric dimethylcyclopropanes. How are the compounds in each pair related (enantiomers, diastereomers, constitutional isomers): A and B; A and C; B and C; C and D?arrow_forwardwhat is the crystallinity of phenazopyridine? with illustationarrow_forwardDraw the structures of the following acids:(a) 2-Ethyl-3-hydroxyhexanoic acid (b) m-Nitrobenzoic acidarrow_forward
- Propose a scheme to separate and isolate a mixture containing 4-aminobenzoate, 1,2,4,5-tetrachlorobenzene, and napthalene. Isolate two of the three solids by extraction. (please explain what solvents to use and the process step by step)arrow_forwardA decapeptide has the following acid composition; Al2,Arg,Cys,Glu,Leu,Phe,Val Partial hydrolysis yield the following tripeptides; Cys-Glu-Leu+Gly-Arg-Cys+Leu-Ala-Ala+Lys-Val-Phe-Gly Reaction of the decapeptide with 2,4-dinitrofluorobenzene yields 2,4-dinitrophenylysine. From the experimental data, deduce the primary structure of the decapeptide. Suggest a scheme you will follow to synthesize the dipeptide Ala-Gly.arrow_forwardExplain why pyrimidine is less basic than pyridinearrow_forward
- Potentiometric titration curve is given below, which is obtained during the potentiometric titration between strong base KOH (0.2 M) with strong acid HI, label the point in the curve from the following options. If more than one points are present than write as x, y(means separate by using comma) a)The point where pH is because of excess OH - ions. b) The point where pH is only because of HI in water. c)The point where [HI]= [I] in water. d)The point where pH=pka e) The point where all HI is neutralized. f) The point where pH corresponds to solution of [I- ] in water. 14 13 12 11 10 9 pH 6. TITIT TITarrow_forwardDraw a Lewis structure for hydroxylamine, NH2OH.arrow_forward2-butanol can be formed as the only product of the Markovnikov addition of H2O to two different alkenes. In contrast, 2-pentanol can be formed as the only product of the Markovnikov addition of H2O to just one alkene. To examine the difference, draw the alkene starting materials of each alcohol. : Draw the bond-line (skeletal) structures of the two alkene starting materials that can be used to synthesize 2-butanol via Markovnikov hydration. Part 1 of 2 Click and drag to start drawing a structure. ☑arrow_forward
- One of these forms of cocaine is relatively insoluble inwater: which form, the free base or the hydrochloride?arrow_forward2-butanol can be formed as the only product of the Markovnikov addition of H2O to two different alkenes. In contrast, 2-octanol can be formed as the only product of the Markovnikov addition of H2O to just one alkene. To examine the difference, draw the alkene starting materials of each alcohol. Draw the bond-line (skeletal) structures of the two alkene starting materials that can be used to synthesize 2-butanol via Markovnikov hydration. Part 1 of 2 Click and drag to start drawing a structure. : ☐ ☑ ⑤arrow_forwardDraw structural formulas for all of the following. Q.) Alcohols with the molecular formula C4H10Oarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- BiochemistryBiochemistryISBN:9781319114671Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.Publisher:W. H. FreemanLehninger Principles of BiochemistryBiochemistryISBN:9781464126116Author:David L. Nelson, Michael M. CoxPublisher:W. H. FreemanFundamentals of Biochemistry: Life at the Molecul...BiochemistryISBN:9781118918401Author:Donald Voet, Judith G. Voet, Charlotte W. PrattPublisher:WILEY
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage LearningBiochemistryBiochemistryISBN:9781305577206Author:Reginald H. Garrett, Charles M. GrishamPublisher:Cengage LearningFundamentals of General, Organic, and Biological ...BiochemistryISBN:9780134015187Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. PetersonPublisher:PEARSON
Biochemistry
Biochemistry
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:W. H. Freeman
Lehninger Principles of Biochemistry
Biochemistry
ISBN:9781464126116
Author:David L. Nelson, Michael M. Cox
Publisher:W. H. Freeman
Fundamentals of Biochemistry: Life at the Molecul...
Biochemistry
ISBN:9781118918401
Author:Donald Voet, Judith G. Voet, Charlotte W. Pratt
Publisher:WILEY
Biochemistry
Biochemistry
ISBN:9781305961135
Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougal
Publisher:Cengage Learning
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Fundamentals of General, Organic, and Biological ...
Biochemistry
ISBN:9780134015187
Author:John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher:PEARSON
GCSE Chemistry - Acids and Bases #34; Author: Cognito;https://www.youtube.com/watch?v=vt8fB3MFzLk;License: Standard youtube license