(a)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(b)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(c)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
(d)
Interpretation:
Compounds with wrong names are given. Correct name for each compound is to be stated.
Concept introduction:
IUPAC has established rules to name an organic compound. Any organic compound has only one name that denotes that compound. The root word determines the number of carbons while counting the longest carbon chain. Double or triple bond should be given lowest carbon number. Whenever possible, the substituent should get lowest number. If more than one substituent is present, prefixes like di, tri, tetra, etc. are used.
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Chapter 22 Solutions
Chemistry with Access Code, Hybrid Edition
- Draw the structural formula for each of the following. a. 3-isobutylhexane b. 2,2,4-trimethylpentane, also called isooctane. This substance is the reference (100 level) for octane ratings. c. 2-tert-butylpentane d. The names given in parts a and c are incorrect. Give the correct names for these hydrocarbons.arrow_forwardThe correct structural for ethyne is: a. HC=CH b. HC=C=H c. HCCH d. H=C=C=Harrow_forwardWhat is the name of this molecule? A. 8-chloro-4-propanyloctyne B. 1-chloro-5-methyl-5-octyne C. 1-chloro-5-octyne D. 7-chloro-3-propyl-1-heptynearrow_forward
- 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-diazacyclohexanearrow_forward1.Draw the condensed structural formula of the following compounds and identify the kind of organic compound they belong to. a. Butanol b. Butanoic acid c. 3-pentanone d. Pentanal e. 4-methyl hexanamine f. 3-chloro-1-pentyne g. Hexanearrow_forward1. Draw a structural diagram for each of the following a. 3-ethyl-4-methyl-1-octene b. 4-propyl-3-methyl-1-heptyne c. 5-ethyl-2,3-dimethylheptane d. 3-ethylhexane e. 3-ethyl-2-methyl-4-propylnonane f. 4-methyl-1-pentyne g. 3-ethyl-2,4-dimethyl-2-pentene h. 3,3-dimethyl-1-pentyne i. cyclooctane j. cycloheptene k. 1,2-dipropylbenzene 1. 1,1-diphenylethane m. 1-butyl-4-methylbenzenearrow_forward
- 1. How many total covalent bonds are present in the compound? (Please refer to the first image attached.) A. 8 B. 10 C. 12 D. 16 2. What is the correct IUPAC name for this compound? (Please refer to the second image attached.) A. 2,5,5-Trimethylhexane B. 2,2,5-Trimethylhexane C. 2,2,5-methylhexane D. 2,5,5-methylhexane 3. Which of the following is a tertiary alcohol? A. 2-Pentanol B. 2-Methyl-2-butanol C. 1-Butanol D. 2-Methyl-1-pentanolarrow_forwardWrite the formula correctly for the following like shown in the image below. 4,4,5-trimethyl-2-hexyne b. Ethylpropanoate c. 3,4-diethyl-2,3,4-trimethyl-1-hexene d. 3-heptanone e. 2,4-dimethyloct-1-ene-3-olarrow_forwardDraw the structures of the following hydrocarbon derivatives. a. Butyl heptanoate b. 3-chloro-4-ethylbenzoic acid c. N,N-diethylpent-3-en-1-amine d. 4-methoxyhept-2-ene e. 3-ethyl-N,2-dimethylhexan-1-amidearrow_forward
- Explain what is wrong with the following organic molecule names, then give the correct name. a. 3-chlorobutane b. 2-pentanal c. 2,3,4-triethyl-hexane d. cis-2-methyl-2-butenearrow_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_forwardWrite a condensed structural formula for each of the following alcohols. a. 2-Methyl-1-propanol b. 4-Methyl-2-pentanol c. 2-Phenyl-2-propanol d. 2-Methycyclobutanolarrow_forward
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