Concept explainers
(a)
Interpretation:
The structure of
Concept introduction:
The root name of the longest carbon chain is the
(b)
Interpretation:
The structure of
Concept introduction:
The root name of the longest carbon chain is the alkane name at the end of the compound’s name. The names of the substituents along with numbers indicate their positions on the longest carbon chain. A prefix of the substituent name shows their numbers. The oxygen atom is attached to the alkyl group. The name of the oxygen atom attached to the alkyl group is alkoxy group.
(c)
Interpretation:
The structure of
Concept introduction:
The root name of the longest carbon chain is the alkane name at the end of the compound’s name. The names of the substituents along with numbers indicate their positions on the longest carbon chain. A prefix of the substituent name shows their numbers. The oxygen atom is attached to the alkyl group. The name of the oxygen atom attached to the alkyl group is alkoxy group.
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Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- Each of the following IUPAC names is incorrect. Explain why it is incorrect and give the correct IUPAC name. a. 2,2-dimethyl-4-ethylheptane b. 5-ethyl-2-methylhexane c. 2-methyl-2-isopropylheptane d. 1,5-dimethylcyclohexane e. 1-ethyl-2,6-dimethylcycloheptane f. 5,5,6-trimethyloctane g. 3-butyl-2,2-dimethylhexane h. 1,3-dimethylbutanearrow_forwardDraw the structure for each compound using wedges and dashed wedges.a. cis-1,2-dimethylcyclopropaneb. trans-1-ethyl-2-methylcyclopentanearrow_forwardChoose the correct IUPAC name for the following structure. Br O A. 7-bromo-3-ethyl-2,5,6-trimethylnonane B. 2-iodo-3-ethyl-7-bromo-di-5,6-methylnonane O C. 7-bromo-3-ethyl-2-iodo6-dimethylnonane. O D. 3-bromo-7-ethyl-8-iodo-4,5-dimethylnonanearrow_forward
- Give the IUPAC name for the chemical in the attached image. [click on attachment to view image if you don't see it] CH3CH₂CH₂CH₂CHCH₂CH₂CH₂CH3 CH3CH₂CH₂ O A. 2,2,5,6-tetraethylhexane B. 2,2,5-triethyloctane O C. 3,6-diethyl-3-methylnonane CH₂CH3 D. 3-ethyl-3-methyl-6-propyldecane CH3arrow_forwardGive the structure corresponding to each IUPAC name. c. 3,5,5-trimethyloctane d. 3-ethyl-4-methylhexane e. 3-ethyl-5-isobutylnonane a. 3-methylhexane b. 3,3-dimethylpentanearrow_forwardWhat is the correct IUPAC name of the following structure? H2C O A. 1,2-epoxy but-4-ene O B. 1,2-epoxy-4-butene O C. 3,4-epoxy-1-butene O D. 2,3-epoxy-1,4-butenearrow_forward
- Match the following IUPAC Name to its appropriate stucture. A. 1,1,2,2,N,N-hexamethylpentane B. 5,6,6-trimethyl-1-heptyne C. 3,3,4,4,5,5-hexamethylpentane D. 2,2,3,3,4,4-hexamethylpentane E. 2,2,3-trimethyl-6-heptyne F. 3-methylbuta-1,2-diene G. 3-methylhexa-1,2-diene H. 3-methylpenta-1,2-dienearrow_forwardWhat is the IUPAC name of this compound ? A. 3-ethyl-2,7,8-trimethylnonane B. 2,6-diisopropyloctane C. 6-ethyl-2-isopropyl-7-methyloctane D. 7-ethyl-2,3,8-trimethylnonane E. 7-isopropyl-2,3-dimethylnonanearrow_forwardIt has been suggested that the following compound was incorrectly named trans-3,5-dimethyl-4- propylnon-3-ene. What is the correct IUPAC name for the compound? A. cis-3,5-dimethyl-4-propylnon-3-ene trans-4(2-hexane)3methylhept-3-ene B. C. trans-4-propyl 3,5-dimethylnon-3-ene D. cis-4(2-hexane)3methylhept-3-ene E. trans-3,5-dimethyl-4-propylnon-3-enearrow_forward
- 4. The names below are incorrect. A reasonable molecular formula can be written to correspond to the incorrect name. After writing the formula give it a correct IUPAC name, and list the errors in the original name. a 2,2-dimethylcyclobutane b. 2-ethyl-4,4-dimethyl-2-pentene 1-ethyl-5-methyl-3-cyclopentene d. 4-isopropyl-m-xylene c. e. 1,4,7-trimethyl-4,6-heptadien-2-ynyl-benzene Jorinationarrow_forwardGive the structure corresponding to each IUPAC name. a. 3-methyl-3-pentanold. 1,3-propanediol b. 4-methyl-2-pentanole. 3,5-dimethylcyclohexanol c. 2,4-dimethyl-2-hexanolf. 6,6-diethyl-4-nonanolarrow_forwardConsider the structure of cyclohexene, if it undergoes epoxidation followed by exposure to water, which of the following final product is formed? a. Cyclohexan-1,2,-diol b. Cyclohexane c. Cyclohexanone d. Hexan-1,-6-dioic acidarrow_forward
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning