Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Textbook Question
Chapter 7, Problem 7.24P
Show how to prepare each compound from 1-heptene.
- a. 1,2-Dichloroheptane
- b. 1-Heptyne
- c. 1-Heptanol
- d. 2-Octyne
- e. cis-2-Octene
- f. trans-2-Octene
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Name the alkyl halide below
CI
a. 4-chlorohexane
O b. chlorohexane
O c. 1-ethyl-1-chlorobutane
O d. 3-chlorohexane
What is the name of the product of this reaction?
a. 2-bromohexane
b. 3,3-dibromohexane
c. 3,4-dibromohexene
d. 1,1-dibromobutane
e. 3,4-dibromohexane
O A. 4-ethyl-5-methyloctane
O B. 4-methyl-5-ethyloctane
OC. 4-methyl-3-propylheptane
O D.4-methyl-5-propyloctane
Chapter 7 Solutions
Organic Chemistry
Ch. 7.2 - Write the IUPAC name of each compound.Ch. 7.2 - Write the common name of each alkyne.Ch. 7.5 - Prob. 7.3PCh. 7.7 - Draw a structural formula for a hydrocarbon with...Ch. 7.7 - Hydration of 2-pentyne gives a mixture of two...Ch. 7.9 - Prob. 7.6PCh. 7 - Prob. 7.7PCh. 7 - Show how to prepare each alkyne from the given...Ch. 7 - Prob. 7.9PCh. 7 - Complete each acid-base reaction and predict...
Ch. 7 - Draw structural formulas for the major product(s)...Ch. 7 - Draw the structural formula of the enol formed in...Ch. 7 - Prob. 7.13PCh. 7 - Prob. 7.14PCh. 7 - Prob. 7.15PCh. 7 - Show reagents and experimental conditions you...Ch. 7 - Show reagents and experimental conditions you...Ch. 7 - Show how to convert 1-butyne to each of these...Ch. 7 - Prob. 7.19PCh. 7 - Show reagents and experimental conditions to bring...Ch. 7 - Show reagents to bring about each conversion.Ch. 7 - Propose a synthesis for (Z)-9-tricosene...Ch. 7 - Propose a synthesis of each compound starting from...Ch. 7 - Show how to prepare each compound from 1-heptene....Ch. 7 - Prob. 7.25PCh. 7 - Prob. 7.26PCh. 7 - Following is the structural formula of the...Ch. 7 - The standard procedure for synthesizing a compound...Ch. 7 - Prob. 7.29PCh. 7 - Prob. 7.30PCh. 7 - Using your reaction roadmap as a guide, show how...Ch. 7 - Using your reaction roadmap as a guide, show how...Ch. 7 - Using your reaction roadmap as a guide, show how...Ch. 7 - Using your reaction roadmap as a guide, show how...Ch. 7 - Prob. 7.35P
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- 3. Choose the correct product of the dehydration of 4,4-dimethyl-3-hexanol(draw out the reaction). A. 4,4-dimethyl-2-hexene B. 3,4-dimethyl-2-hexene C. 4,4-dimethyl-1-hexene D. 3,3-dimethyl-4-hexene A B.arrow_forwardA student was given the structural formulas of several compounds and was asked to give them systematic names. How many did the student name correctly? Correct those that are misnamed. a. 4-bromo-3-pentanol b. 2,2-dimethyl-4-ethylheptane c. 5-methylcyclohexanol d. 1,1-dimethyl-2-cyclohexanol e. 5-(2,2-dimethylethyl)nonane f. isopentylbromide g. 3,3-dichlorooctane h. 5-ethyl-2-methylhexane i. 1-bromo-4-pentanol j. 3-isopropyloctane k. 2-methyl-2-isopropylheptane l. 2-methyl-N,N-dimethyl-4-hexanaminearrow_forwardO A. 1,1-dimethyl-1,4-pentadiene B. 2-methyl-2,5-hexadiene OC.5,5-dimethyl-1,4-pentadiene O D.5-methyl-1,4-hexadienearrow_forward
- 4- Choose the correct reactants required to synthesize the following molecule. H3CO OCH 3 A. Acetone and methanal B. Acetone and methanol C. Formaldehyde and propanal D. Formaldehyde and propanol 5- What is the IUPAC name of the following compound? CI A. 6-Chloro-4-ethoxy-1-octanal B. 6-Chloro-4-ethoxyoctanal C. 6-Chloro-4-ethoxycyclooctanal D. 4-Ethoxy-6-chlorooctanal - What is the IUPAC name of the following compound? 0 Br. Br Cl A. 2,6-Dibromo-3-chloro-5,5-dimethylhexanone B. 2,6-Dibromo-3-chloro-5,5-dimethylcyclohexanone C. 2,6-Dibromo-5-chloro-3,3-dimethylhexanone D. 2,6-Dibromo-5-chloro-3,3-dimethylcyclohexanonearrow_forwardConsider the following starting material and choose all of the functional groups that are likely to oxidize in it. a. aldehyde b. secondary alcohol c. alkane d. hemiacetal e. carboxylic acid f. alkenearrow_forwardWhat is the IUPAC name for CH 3 -CH 2 - CH 2-I a. diiodopropane. b. propane diiodide. c. 1-iodopropane. d. 3-iodopentane. e. 3-iodopropane.arrow_forward
- a. Name the hydrocarbons in the reaction.b. Circle and identify the functional group in the hydrocarbons.arrow_forwardDraw the structure for following compounds. A. 1,3-dichlorocyclohexane B. 2-bromo-3,3-dimethylpentanearrow_forward29. Which of these generic structures denotes an alcohol? E. I F. RCOH G. I RCR A. R-CI B. R-OH C. R-O-R' D. R-NH-R' RCH 30. Which of the generic structures denotes a carboxylic acid? E. I RCH F. I RCOH G. RCR A. R-CI B. R-OH C. R-O-R' D. R-NH-R' 31. Which of these generic structures denotes an aldehyde? E. RCH F. I RCOH A. R-CI B. R-OH C. R-O-R' D. R-NH-R' RCR G.arrow_forward
- What is the product of a reaction between 1-bromoethane with ammonia? A. acetonitrile B. ethanamine C. ethyl ethanoate D. ethanolarrow_forwardConsider the attached picture: 1. What specific reaction is involved? a. nitration b. alkylation c. halogenation d. acylation 2. What type of reaction is involved? a. Addition Reaction b. Elimination Reaction c. Substitution Reaction 3. What are the products? a. chlorocyclohexane and hydrochloric acid b. chlorocyclobenzene and hydrochloric acid c. 1-chloro-1,3,5-cyclohexatriene and hydrochloric acid d. chlorobenzene and hydrochloric acidarrow_forward29. The correct name for the compound CH3-CH₂-CH2-O-CH₂-CH3 is A. 3-hexanol B. ethyl propyl ether C. 3-pentanol D.3-ether pentane TOOarrow_forward
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