Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 14.3B, Problem 14.4P
Give a common name (when possible) and a systematic name for each compound.
- a. CH3OCH=CH2
- b. CH3CH2OCH(CH3)2
- c. ClCH2CH2OCH3
- h. CH3C ≡ CCH2OCH3
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
33. What is each compound's systematic name?
a. CH₂C=CCH₂CHCH, b. CH₂C=CCH₂CHCH₂
Br
CH₂CH₂CH₂
CH₁
c. CH₂C=CCH₂CCH, d. CH₂CHCH₂C=CCHCH
CH,
CH,
Name each alkyne.
a. CH=C-CH-CH3
CH3
b. CH3-C=C-CH-CH-CH,-CH,
CH3
CH3
c. CHEC-C-CH,-CH3
CH2
ČH,
CH3
d. CH;-C=C-CH-C-CH,
CH2 CH3
ČH3
Which compound is a likely product from addition of Cl2 to 1-butene?
a.
ClCH2CH2CH2CH2Cl
b.
CH3CH2CHClCH2Cl
c.
CH3CH2CH2CHCl2
d.
CH3CH2CCl2CH3
Chapter 14 Solutions
Organic Chemistry (9th Edition)
Ch. 14.2C - Rank the given solvents in decreasing order of...Ch. 14.2D - Prob. 14.2PCh. 14.2D - In the presence of 18-crown-6, potassium...Ch. 14.3B - Give a common name (when possible) and a...Ch. 14.3C - Prob. 14.5PCh. 14.3C - Name the following heterocyclic ethers.Ch. 14.4 - Propose a fragmentation to account for each...Ch. 14.5 - Prob. 14.8PCh. 14.5 - Prob. 14.9PCh. 14.6 - Prob. 14.10P
Ch. 14.7 - Explain why bimolecular condensation is a poor...Ch. 14.7 - Prob. 14.12PCh. 14.7 - Prob. 14.13PCh. 14.8 - Prob. 14.14PCh. 14.8 - Prob. 14.15PCh. 14.8 - Prob. 14.16PCh. 14.10A - Prob. 14.17PCh. 14.10A - Prob. 14.18PCh. 14.10B - Prob. 14.19PCh. 14.11B - Show how you would accomplish the following...Ch. 14.11B - Prob. 14.21PCh. 14.12 - Prob. 14.22PCh. 14.12 - Prob. 14.23PCh. 14.12 - Prob. 14.24PCh. 14.13 - Prob. 14.25PCh. 14.13 - Prob. 14.26PCh. 14.14 - Prob. 14.27PCh. 14.15 - Give the expected products of the following...Ch. 14 - Write structural formulas for the following...Ch. 14 - Give common names for the following compounds. a....Ch. 14 - Give IUPAC names for the following compounds. a....Ch. 14 - Glycerol (propane-1,2,3-triol) is a viscous syrup...Ch. 14 - Prob. 14.33SPCh. 14 - Show how you would make the following ethers,...Ch. 14 - (A true story.) An inexperienced graduate student...Ch. 14 - Prob. 14.36SPCh. 14 - a. Show how you would synthesize the pure (R)...Ch. 14 - a. Predict the values of m/z and the structures of...Ch. 14 - The following reaction resembles the...Ch. 14 - Prob. 14.40SPCh. 14 - Prob. 14.41SPCh. 14 - Prob. 14.42SPCh. 14 - Give the structures of the intermediates...Ch. 14 - Prob. 14.44SPCh. 14 - Show how you would synthesize the following ethers...Ch. 14 - Prob. 14.46SPCh. 14 - Prob. 14.47SPCh. 14 - Prob. 14.48SPCh. 14 - An acid-catalyzed reaction was carried out using...Ch. 14 - Propylene oxide is a chiral molecule. Hydrolysis...Ch. 14 - Prob. 14.51SPCh. 14 - Prob. 14.52SPCh. 14 - Prob. 14.53SPCh. 14 - Prob. 14.54SPCh. 14 - In 2012, a group led by Professor Masayuki Satake...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- CH2 H3C H3C COOH Reagents e. PB13 f. NaCN then H3O* g. NBS, CCI4 h. CrO3, H2SO4 а. HBr b. Mg, ether c. CO2, ether then H3O* d. BH3, THF then H2O2, OH"arrow_forwardDraw the products formed when CH3CH2C ≡ C−Na+reacts with each compound. a. CH3CH2CH2Brb. (CH3)2CHCH2CH2Clc. (CH3CH2)3CCld. BrCH2CH2CH2CH2OHe. ethylene oxide followed by H2Of. propene oxide followed by H2Oarrow_forwardA. Naming Structures 1. Use the JUPAC rules to name the following structures. CH CH = CHCHCH, b. CH3 a. CH3 CH2 CH3 CH-CH сн, CH3CHCH2CH =CHCCH, CH3 2. Use IUPAC rules to name the following structures. CH,CH3 b. CH3 CH3 CH3 CH,CH, CH3CH, В. B. Draw the structures of the following cycloalkanes 1. 2,3-dimethyl-5-propyldecane 2. 3,4,5-triethyloctane 3. 1-ethyl-3-propylcyclopentane 4. 1,2,2,4-tetramethylcyclohexanearrow_forward
- Name each alkene. a. CH;=CH-CH;-CH3 CH, CH3 b. CH3-CH-c=CH-CH3 c. CH,=HC-CH–CH,-CH,-CH, CH3-CH ČH3 CH3 d. CH3-CH-CH=C-CH3 CH,-CH3arrow_forward1. Provide proper IUPAC names for the following compounds. a. CH3 | CH3C CCHCH2CH2CH3 CH3 Br b. H₂C=CH-C-CH-CC-H | CH3 C.arrow_forward6. What is the product? CH3 осно A. C. A and B A. A B. B C. C CH3 B. DBN CH₂arrow_forward
- Draw all the isomers that have molecular formula C5H11Br. a. Give the systematic name for each of the isomers. b. Give a common name for each isomer that has a common name. c. How many of the isomers are primary alkyl halides? d. How many of the isomers are secondary alkyl halides? e. How many of the isomers are tertiary alkyl halides?arrow_forwardIndicate the product obtained by reacting A and B. A || H3C-S-CH₂ Na* || CH 3 B CH2. C. CH3 H3C CH3arrow_forward4. Use the IUPAC Nomenclature System to name each of the following compounds: a. b. CH,CCH₂CH, 0 HCCHCH₂CH₂ CI O -C-C-CH₂ Br CHỊCH,CH,CH, CH,CCH₂CH₂CH CH, CI CH₂CHCH₂CH Br CH, Ô CH,CCH.CCH.CH.CH, OH 0 CH₂ CH,CCH₂CH.CH,CHCH,C-H H,CHCH.CH CH₂arrow_forward
- a. The following compounds have the same molecular formula as benzene. How many monobrominated products could each form? 1. HC‚CC‚CCH2CH3 2. CH2“CHC‚CCH“CH2 b. How many dibrominated products could each of the preceding compounds form? (Do not include stereoisomers.) c. How many dibrominated products could each of the compounds form if stereoisomers are included?arrow_forwardName each compound in which the benzene ring is best treated as a substituent. CH3 a. CH3-CH-CH,-CH-CH,-CH–CH,-CH; CH,-CH3 b. CH,-CH-CH=CH-CH,-CH,–CH,-CH, c. CH3-C=C-CH-CH-CH-CH2-CH3 CH3 CH3arrow_forwardWhat is the major product for each of the following reactions? (If an enol is created, write both the enol and keto products. If both ortho and para products are made, write both.)arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY