Concept explainers
(a)
Interpretation: The structure corresponding to the given IUPAC name is to be stated.
Concept introduction: One should follow the given steps to derive the structure of an
(b)
Interpretation: The structure corresponding to the given IUPAC name is to be stated.
Concept introduction: One should follow the given steps to derive the structure of an aldehyde from its IUPAC name. The first step is finding of longest parent chain that contains an aldehyde group. The second step is changing of -e ending of the parent alkane to the suffix -al. However, when an aldehyde
(c)
Interpretation: The structure corresponding to the given IUPAC name is to be stated.
Concept introduction: One should follow the given steps to derive the structure of an aldehyde from its IUPAC name. The first step is finding of longest parent chain that contains an aldehyde group. The second step is changing of -e ending of the parent alkane to the suffix -al. However, when an aldehyde
(d)
Interpretation: The structure corresponding to the given IUPAC name is to be stated.
Concept introduction: One should follow the given steps to derive the structure of an aldehyde from its IUPAC name. The first step is finding of longest parent chain that contains an aldehyde group. The second step is changing of -e ending of the parent alkane to the suffix -al. However, when an aldehyde
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Organic Chemistry-Package(Custom)
- Draw the structure corresponding to each IUPAC name (specifically, D-F please)arrow_forwardGive the structure corresponding to each IUPAC name.a. 2-isobutyl-3-isopropylhexanalb. trans-3-methylcyclopentanecarbaldehydec. 1-methylcyclopropanecarbaldehyded. 3,6-diethylnonanalarrow_forward1. Give the structure corresponding to each name. a. 4-ethyl-3-heptanol b. 3-chloro-1,2-propanediol c. diisobutyl ether d. 1,2-epoxy-1,3,3-trimethylcyclohexane e. 1-ethoxy-3-ethylheptanearrow_forward
- Give the structure corresponding to each IUPAC name. a. 2-methoxypropane b. cyclobutyl ethyl ether c. 1-ethoxy-2-ethylcyclohexane d. butyl chloride e. 2-methylcyclohexanethiol f. 1-ethyl-2-fl uorocyclobutanearrow_forward17. CH2CH3 The correct name for the compound given above is which of the follow ing? a. 1-propyl-3-ethy-4-methylbenzene b. 4-cyclopropy-2-ethyl-1-methy lbenzene c. p.o - methyl, ethyleyclopropylbenzene d. 1-propyl-3-ethyl-4-methyleyclohexane 18. The correct structure for 1,4-dicyc lopropyleyc lohexane is which of the following? a. CH3-CH2-CH2- b. CH2 CH2-CH3 с. CH,-CH2-CH2 CH-CH, CH d.arrow_forwardGive the IUPAC name for each compound. CH3 CH2CH3 Br a. PHCH(CH3)2 b. С. d.arrow_forward
- Give 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_forwardDraw the structure of the ff. aldehydes and ketones. a. 3-chlorobutanal 6. 8,8-dibromo -4-cthylcyclo hexanone C. 2,4-dimetnylpontanone • Draw the structure of the ff. compounds. a. oyclobutanecarboxylic acid b. 3,8-dimcthylpontancdioic acid C. 4-aminopcntanoic acid d. 2-mothylcycloheranecarooxylic acid m- chlorobėnzoic acidarrow_forwardDraw the structure corresponding to each IUPAC name. a.3-ethyl-2-methylhexane b. sec-butylcyclopentane c.4-isopropyl-2,4,5-trimethylundecane d.cyclobutylcycloheptane e.3-ethyl-1,1-dimethylcyclohexane f. 4-butyl-1,1-diethylcyclooctane g.6-isopropyl-2,3-dimethyldodecane h. 2,2,6,6,7-pentamethyloctane i. cis-1-ethyl-3-methylcyclopentane j. trans-1-tert-butyl-4-ethylcyclohexanearrow_forward
- Cyclopentanone is treated with chlorine (Cl2) in the presence of acid (H*). What product is formed? A. Chlorocyclopentane B. 1-chloro-1-hydroxycyclopentane C. 2-chlorocyclopentanone D. 3-chlorocyclopentanonearrow_forwardPls help ASAParrow_forwardWhat is the IUPAC name for the following compound? CH₂CH₂ C CH3-CH₂-CH-CH₂-CH-CH-CH-CH₂ CI CH3 Select one: O A. 3,7-dichloro-5-ethyl-6-methyloctane O B. 2-chloro-3-methyl-4-(2-chlorobutyl) hexane O C. 2,6-dichloro-4-ethyl-3-methyloctane O D. 3-chloro-5-(2-chloro-1-methylpropyl) heptane OE. 2,3,4,6-dichloroethylmethyoctanearrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning