a. 3-ethyl-2-methylhexane b. sec-butylcyclopentane f. 4-butyl-1,1-diethylcyclooctane g. 6-isopropyl-2,3-dimethylnonane c. 4-isopropyl-2,4,5-trimethylheptane h. 2,2,6,6,7-pentamethyloctane d. cyclobutylcycloheptane i. cis-1-ethyl-3-methylcyclopentane e. 3-ethyl-1,1-dimethylcyclohexane j. trans-1-tert-butyl-4-ethylcyclohexane

a. 3-ethyl-2-methylhexane b. sec-butylcyclopentane f. 4-butyl-1,1-diethylcyclooctane g. 6-isopropyl-2,3-dimethylnonane c. 4-isopropyl-2,4,5-trimethylheptane h. 2,2,6,6,7-pentamethyloctane d. cyclobutylcycloheptane i. cis-1-ethyl-3-methylcyclopentane e. 3-ethyl-1,1-dimethylcyclohexane j. trans-1-tert-butyl-4-ethylcyclohexane

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Draw a structure a. 3,4-dimethylpent-1-yneb.3-methyl-3-ethyl-1-butenec. 3,3-dimethyl-4-decened.1,1-dimethyl-4-ethyl-2,5-cyclohexadienee. 4-ethyl-2,3-dimethyl-2-heptenef. 1-chlorocyclopropeneg. 2,6-dimethyl-2,5-octadieneh. 1-cyclobutyl-3-methyl-1-butynei. 5-bromo-2-chlorotoluene
Draw the structure of the following compounds. a. 1-ethyl-3-methylcycloheptane b. Cyclopropylcyclopentane c. 1,1-diethyl-4-(3,3-dimethylbutyl)cyclohexane
O A. 4-ethyl-5-methyloctane O B. 4-methyl-5-ethyloctane OC. 4-methyl-3-propylheptane O D.4-methyl-5-propyloctane
Draw structures for each of the following carbonylcompounds.a. 2,2-dichloro-3-pentanoneb. 4-methylpentanalc. isopropyl hexanoated. octanoamidee. 3-fluoro-2-methylbutanoic acidf. cyclopentanalg. hexyl methanoate
1. Structure of 4-ethyl-2 - methyl hexyl cyclooctane. 2. Structure of 4-ethyl-2 - methyl hexyl cycloctane
13. Ethylethanoate and butanoic acid can be classified as A. positional isomers B. chain isomers C. functional isomers D. stereoisomers 14. Which of the following pairs are positional isomers A. trans-1,4-dichlorocyclohexane, cis-1,3-dichlorocyclopentane B. trans 1,4-dichlorocyclohexane, cis-1,4-dichlorocyclohexane C. 2-pentanol, Cyclopentanol D. 1,2-cycohexanediol, 1,3-cycohexanediol 15. Which of the following compounds will have zero dipole moment? A. cis-1,2-dibromoethylene B. 1,1-dibromoethylene C. trans-1,2-dibromoethylene D. all of these 16. Which of the following is not aromatic: A. cyclopentadienyl cation B. cyclopentadienyl anion C. Cyclopropenyl cation D. Cycloheptatrienyl cation 17. Which of the following compounds containing lone pair has the least tendency to donate its electrons? A. the lone pair in pyridine B. the lone pair in furan C. the lone pair in pyrole D. the lone pair in thiophene
This is no multiple questions please answer only draw structure all
Based on the image attached, what is the name of the compound? A. 3-chloro-2-ethylpyrimidine B. 3-chloro-2-ethyl-1,4-diazacyclohexane C. 3-chloro-2-ethylcyclohexan-1,4-diamine D. 2-chloro-3-ethyl-1,4-diazacyclohexane
Draw structures for the following: a. 4-Isopropyl-3-ethynonane b. 4-Ethyl-2,2-dimethylhexane c. 2,4,4-Trimethylheptane d. 4-Methylheptane 4-Ethyl-3,4-dimethylhexane f. 3,3-Diethyl-2,5-dimethylnonane е.
A 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-hexanamine
XIII. Draw skeletal structures corresponding to the following names. a. 1-chloro-2-isopropylcyclopentane b. 3,5-dicyclohexylnonane c. 3,3-Diethyl-2,5-dimethylnonane d. 4-Isopropyl-3-methylheptane
12. Which of the following structural formulas shows a compound that is an isomer of butane? C. e. H 110-4 H H III H - H c. alkyl halides d. amines e. ethers H н-с HIC CIC-H 'H HIC-H T 4 * ΗΗΗΗ H-C-C-C-C-O-H ΗΗΗΗ b. H-C # H- C-H H H d. H HIĊIC= H H H 13. Which class of organic molecules can form directly from alkanes? a. alcohols b. ketones H -C-H