Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 4, Problem 8PP
Practice Problem 4.8
Give names for the following substituted
(a)
(b)
(c)
(d)
(e)
(f)
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Write the systematic names of the following alkanes.
(a) CH3CH2CH2CH2CH3(b) CH3−CH3(c) CH3−CH2–CH2−CH3(d) CH3−CH2–CH2−CH2–CH2−CH2–CH2−CH3(e) CH4(f) CH3CH2CH3
Write structural formulas for all the constitutionally isomeric compounds having the given molecular formula.(a) C4H10(b) C5H12(c) C2H4Cl2(d) C4H9Br(e) C3H9N
2.35
Write a structural formula for each of the following compounds:
(a) 6-Isopropyl-2,3-dimethylnonane
(b) 4-tert-Butyl-3-methylheptane
(c) 4-Isobutyl-1,1-dimethylcyclohexane
(d) sec-Butylcycloheptane
(e) Cyclobutylcyclopentane
Chapter 4 Solutions
Organic Chemistry
Ch. 4 - Prob. 1PPCh. 4 - Which structure does not represent...Ch. 4 - Prob. 3PPCh. 4 - Draw bond-line formulas for all of the isomers of...Ch. 4 - Prob. 5PPCh. 4 - Draw bond-line formulas and give IUPAC...Ch. 4 - Draw bond-line formulas and give IUPAC...Ch. 4 - Practice Problem 4.8 Give names for the following...Ch. 4 - Prob. 9PPCh. 4 - Prob. 10PP
Ch. 4 - Prob. 11PPCh. 4 - Give the structures and IUPAC names for all the...Ch. 4 - Prob. 13PPCh. 4 - Practice Problem 4.14 Show by a calculation (using...Ch. 4 - Practice Problem 4.15 Write structures for the cis...Ch. 4 - Practice Problem 4.16
(a) Write structural...Ch. 4 - Practice Problem 4.17 Write a conformational...Ch. 4 - Practice Problem 4.18
(a) Write the two...Ch. 4 - Prob. 19PPCh. 4 - Practice Problem 4.20 (a) What is the index of...Ch. 4 - Practice Problem 4.21
Zingiberene, a fragrant...Ch. 4 - Practice Problem 4.22 Carbonyl groups also count...Ch. 4 - Prob. 23PCh. 4 - Give systematic IUPAC names for each of the...Ch. 4 - Prob. 25PCh. 4 - Write the structure and give the IUPAC systema.tic...Ch. 4 - 4.27. Write the structure(s) of the simplest...Ch. 4 - Prob. 28PCh. 4 - 4.29. Write structures for the following...Ch. 4 - Prob. 30PCh. 4 - A spiro ring junction is one where two rings that...Ch. 4 - 4.32. Tell what is meant by a homologous series...Ch. 4 - Four different cycloalkenes will all yield...Ch. 4 - 4.34. (a) Three different alkenes yield...Ch. 4 - Prob. 35PCh. 4 - Prob. 36PCh. 4 - 4.37. Write the structures of two chair...Ch. 4 - Prob. 38PCh. 4 - Without referring to tables, decide which member...Ch. 4 - Prob. 40PCh. 4 - 4.41. Which compound would you expect to be the...Ch. 4 - Prob. 42PCh. 4 - 4.43. Write the two chair conformations of each of...Ch. 4 - Provide an explanation for the surprising fact...Ch. 4 - Prob. 45PCh. 4 - 4.46. Specify the missing compounds and/or...Ch. 4 - Consider the cis and trans isomers of...Ch. 4 - Prob. 48PCh. 4 - Open the energy-minimized 3D Molecular Models on...Ch. 4 - 4.50. Open the 3D Molecular Models on the book’s...Ch. 4 - 4.51. Open the 3D Molecular Model on the book’s...Ch. 4 - 1. The predominant conformation for D-glucose is...Ch. 4 - Prob. 2LGPCh. 4 - When 1,2-dimethylcyclohexene is allowed to react...Ch. 4 - Prob. 4LGP
Additional Science Textbook Solutions
Find more solutions based on key concepts
Distinguish between microevolution, speciation, and macroevolution.
Campbell Essential Biology (7th Edition)
APPLY 1.2 Express the following quantities in scientific notation
using fundamental SI units of mass and lengt...
Chemistry (7th Edition)
Dr. Ara B. Dopsis and Dr. C. Ellie Gans are performing genetic crosses on daisy plants. They self-fertilize a b...
Genetic Analysis: An Integrated Approach (3rd Edition)
Where is transitional epithelium found and what is its importance at those sites?
Anatomy & Physiology (6th Edition)
a. Which compound has the stretching vibration for its carbonyl group at the highest frequency: acetyl chloride...
Organic Chemistry (8th Edition)
Match each of the following items with all the terms it applies to:
Human Physiology: An Integrated Approach (8th Edition)
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
- The skeletal line formula for a branched alkene is shown below. (i) What is the molecular formula of this compound? (ii) How many carbon atoms are in the longest chain, ignoring the double bond? (iii) What is the longest chain incorporating both carbons of the double bond? (iv) How many substituents are on this chain? (v) Give the IUPAC name for this compound. [6]arrow_forwardWrite structural formulas for compounds that meet the following descriptions:(a) A 6-carbon alkene whose longest chain is 4 carbons inlength (three possibilities)(b) An alkyne with 5 carbons total (three possibilities)(c) A monosubstituted benzene with a total of 8 carbons(one possibility)(d) A disubstituted benzene with a total of 8 carbons(three possibilities)arrow_forwardGive the systematic (IUPAC) names of the following alkenes. (а) СH— CH— CH— CH(CH3)2 (b) CH3(CH2)3¬C-CH2CH3 CH2 (c) CH2=CH-CH,–CH=CH2 (d) CH, —С—CH—CH—СH, CH3 (е) (f) (g) CH3 CH2 CH3 (h) .CH3 (j)arrow_forward
- 1. Write condensed structural formula for all isomers of compounds that fulfill the following requirements: (a) Alkenes with molecular formula CsH10. (b) Alkynes with molecular formula C4H6. (c) Dienes with molecular formula C4H6. 2. For each of the following, give the order of increasing boiling point: (a) n-Heptane, n-octane and n-hexane. (b) n-Pentane, isopentane and n-hexane. (c) 2-Methylhexane, n-heptane and 3,3-dimethylpentane. 9 3. Isomeric compounds can sometimes be distinguished by observing the number of mono- brominated compounds that each forms. In the following cases decide which isomer is present by the number of compounds that are formed. (a) Compound A forms four monobromo compounds. Is it 2-methylbutane or n-pentane? (b) CompoundB forms four monobromo compounds. Is it 2- methylpentane or 3- methylpentane? (c) Compounds C forms monobromo compound. Is it cyclopentane or one mehtylcyclopentane? 4. A hydrocarbon C5H12 was allowed to react with bromine. Only monobromo…arrow_forwardHi, need help with a & barrow_forwardFor each of the following compounds, identify all groups that would be considered substituents and then indicate the systematic name for each compound. (a) (b) (d) (e)arrow_forward
- on 2.39 Using the method outlined in Section 2.17, give an IUPAC name for each of the following alkyl groups, and classify each one as primary. secondary, or tertiary: (a) CH₂(CH₂CH₂- (b)-CH,CH,CHCH,CH,CH, CH,CH, (c)-C(CH₂CH₂) (d) -CHCH,CH,CH, (0) B) -CH₂CH₂- CH- CH₂arrow_forwardWhich of the following is true about the carbon-carbon single bond in 1,3-butadiene when compared to the carbon-carbon single bond in ethane? (A) It is shorter than the carbon-carbon single bond of ethane. (B) The single bond in 1,3-butadiene has a higher %s character than in ethane The hydrogen atoms push the carbons closer using electrocyclic forces. Both A and B. (E) None of the above.arrow_forwardPLEASE PROVIDE EXPLANATION THANK YOU.....arrow_forward
- If either of the following molecules has a stereogenic carbon (chirality center), give structures for both of the enantiomers. (a) 2-bromopropane (b) 2-bromobutanearrow_forwarda) Draw structures for the following compounds. (i) (ii) (iii) 3-ethyl-4-methylhexane 4-tert-butyl-2-methylheptane 3-methylpent-1-ene (b) Provide the IUPAC names for the following (i) (ii) (CH3)3C(CH2)3CH(CH₂CH3)CH₂CH₂CH3arrow_forwardGive the systematic (IUPAC) names of the following alkenes. (d) CH2=C=CH-CH=CH2 CH3 (e) (f) (g) CH3 CH2 CH3 (h) .CH3 (j)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
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License