Fundamentals of General, Organic, and Biological Chemistry (8th Edition)
8th Edition
ISBN: 9780134015187
Author: John E. McMurry, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Textbook Question
Chapter 16.2, Problem 16.1P
Identify the following compounds as primary, secondary, or tertiary
- (a) CH3(CH2)4CH2NH2
- (b) CH3CH2CH2NHCH(CH3)2
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
What is the IUPAC name of the following compound? (No need to provide E/Z
designation.)
CO₂H
When pentane is exposed to Br2 in the presence of light, a halogenation reaction occurs. Write the formulas of:(a) All possible products containing only one bromine(b) All possible products containing two bromines that are not on the same carbon
Draw the structures of the following acids:(a) 2-Ethyl-3-hydroxyhexanoic acid (b) m-Nitrobenzoic acid
Chapter 16 Solutions
Fundamentals of General, Organic, and Biological Chemistry (8th Edition)
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
- Draw all possible carboxylic acids with the formula C5H10O2.arrow_forwardWrite the IUPAC name for each unsaturated hydrocarbon. (a) CH,=CH(CH,),CH3 CH3 CH3 H,C- (b) CH3 (c) CH3 alaTTarrow_forwardDraw structural formulas for all of the following. Q.) Alcohols with the molecular formula C4H10Oarrow_forward
- b) Determine which ionization state corresponds to aspartic acid (shown below) at pH 1, 7, and 10 by selecting the most suitable answer from the statements i-iv. The pK of the amine, carboxylic acid, and side chain of aspartic acid are 9.6, 1.88 and 3.65, respectively. ОН ÓH ÑH2 i) the amine is charged; the carboxylic acids are neutral. ii) the amine and carboxylic acids are all charged. iii) the amine is neutral, and the carboxylic acids are charged. iv) the amine and the carboxylic acids are all neutral. pH Statement (i, ii, iii, or iv) 1 7 10 %3Darrow_forwardIdentify the acid on the left and its conjugate base on the right in the following equations:(a) HOCl + H2O ↔ H3O+ + OCl-(b) HONH2 + H2O ↔ HONH3+ + OH-(c) NH4+ + H2O ↔ NH3 + H3O+(d) 2HCO3-2 ↔ H2CO3 + CO3-2 (e) PO4-3 + H2PO4- ↔ 2HPO4-2arrow_forwardDrawn 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_forward
- Each of the following materials has an ester that is responsible for its smell and/or flavor. Search the internet and determine what that ester is, draw its structure, and what carboxylic acid and alcohol are used to form it.(a) Juicy Fruit gum flavoring(b) Peach odor(c) Apple odor(d) Rum odorarrow_forwardIDENTIFY THE FUNCTIONAL GROUP PRESENT IN THESE COMPOUNDS. A = ? B = ? C = ?arrow_forwardDraw the structures of the following compounds. (Includes both new and old names.) 3-cyclopentylhexan-3-olarrow_forward
- Carvone exists as a pair of enantiomers. (R)-(-)-carvone smells like spearment, whereas (S)-(+)-carvone smells like caraway. Why do these enantiomers have different smells (i.e., different biological activity) ?arrow_forwardIn the preparation of aspirin, You can do the functional group test to ensure the completion of the reaction. (a) What is the name of reagent used? (b) What is your observation if any unreacted starting material is present? (c) What is the name of the functional group responsible for this reaction?arrow_forwardIdentify the conjugate acids and bases in the following pairs of substances. (CH3)3NH / (CH3)3N *H3NCH2CH,C00 / H2NCH;CH2COO OOCCH,COOH/ 00CCH2CO0arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
GCSE Chemistry - Acids and Bases #34; Author: Cognito;https://www.youtube.com/watch?v=vt8fB3MFzLk;License: Standard youtube license