a) p-bromochlorobenzene
Interpretation:
The structure of the compound with IUPAC name p-bromochlorobenzene is to be given.
Concept introduction:
Disubstituted benzenes are named using the prefixes ortho (o), meta (m) and para (p). An ortho-disubstituted benzene has its two substituent groups in a 1,2-relationship on the ring. A meta-disubstituted benzene has its two substituent groups in a 1,3-relationship on the ring. A para-disubstituted benzene has its two substituent groups in a 1,4-relationship on the ring. While writing the name the substituent groups are arranged alphabetically.
To draw:
The structure of the compound with IUPAC name p-bromochlorobenzene.
b) p-bromotoluene
Interpretation:
The structure of the compound with IUPAC name p-bromotoluene is to be given.
Concept introduction:
Compounds with an amino group attached to a benzene ring are named as a derivative of aniline. Substituted anilines are named using the prefixes ortho (o), meta (m) and para (p). An ortho-substituted aniline has an another substituent in a 1,2-relationship on the ring. A meta-disubstituted aniline has an another substituent in a 1,3-relationship on the ring. A para-disubstituted aniline has another substituent in a 1,4-relationship on the ring.
To draw:
The structure of the compound with IUPAC name p-bromotoluene.
c) m-chloroaniline
Interpretation:
The structure of the compound with IUPAC name m-chloroaniline is to be given.
Concept introduction:
Compounds with an amino group attached to a benzene ring are named as a derivative of aniline. Substituted anilines are named using the prefixes ortho (o), meta (m) and para (p). An ortho-substituted aniline has an another substituent in a 1,2-relationship on the ring. A meta-disubstituted aniline has an another substituent in a 1,3-relationship on the ring. A para-disubstituted aniline has another substituent in a 1,4-relationship on the ring.
To draw:
The structure of the compound with IUPAC name m-chloroaniline.
d) 1-chloro-3,5-dimethylbenzene
Interpretation:
The structure of the compound with IUPAC name 1-chloro-3,5-dimethylbenzene is to be given.
Concept introduction:
Benzene with more than two substituent groups are named choosing a point of attachment ac carbon 1 and numbering the substituent groups on the ring so that the second substituent has as low number as possible. If ambiguity still exists, numbering is done such that the third and fourth substituent groups have a number as low as possible, until a point of difference is obtained. While writing the name the substituent groups are arranged alphabetically.
To draw:
The structure of the compound with IUPAC name 1-chloro-3,5-dimethylbenzene.
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Chapter 15 Solutions
ORGANIC CHEMISTRY W/OWL
- Can you help me and explain the answers please.arrow_forwardB 1 of 2 Additional problems in preparation to Midterm #1: 1.) How can the following compounds be prepared using Diels-Alder reaction: CH3 O CN (a) (b) CN CH3 2.) What is the missing reagent in the shown reaction? H3C + ? H3C H3C CN H3C ''CN (၁) H 3.) Write the products 1,2-addition and 1,4-addition of DBr to 1,3-cyclohexadiene. Remember, D is deuterium, a heavy isotope of hydrogen. It reacts exactly like hydrogen. 4.) In the shown reaction, which will be the kinetic product and which will be the thermodynamic product? H3C CI H3C HCI H3C + 5.) Which of the following molecules is aromatic? (a) (b) (c) H 6.) Which of the following molecules is aromatic? (a) (b) (c) 7.) Write the mechanism for the shown reaction. + Ха AICI 3 CI 8.) Suggest reagents that would convert benzene into the shown compounds. CI NO2 -8-6-6-8-a (a) (b) (c) (d) (e) (a) SO3H Brarrow_forwardThe number of 2sp^2 hybridized atoms in is: A. 8; B. 6; C.4; D.2; E.0;arrow_forward
- The highest boiling compound from among the following isA. 2-methylheptane; B. 3-methylheptane; C. 2,2-dimethylhexane;D. octane; E. 2,2,3-trimethylpentanearrow_forwardWhich of the following features are found in the most stable structure ofCH5NO that does not have a CO bond?w. a π bond, x. two NH bonds, y. one OH bond, z. 3 lone pairsA. w, x; B. x, y; C. y, z; D. x, y, z; E. all of them.arrow_forwardWhich one of the following functional groups is not present in thecompound shownA. amine; B. aldehyde, C. ether; D. amide. E. ketonearrow_forward
- Which of the following formulas correspond to at least one compound inwhich resonance is important?w. C2H5N x. C3H5Br; y. C3H4; z. C4H6.A. w, x, y; B. x, y, z; C. w, x, z; D. w, y, z; E. all of themarrow_forwardPredict the product(s) that are formed after each step for reactions 1-4. In each case, consider formation of any chiral center(s) and draw all expected stereoisomers. 1) OH 1) HBr (SN2) 2) NaOH, heat 3) BH3, THF 4) H2O2, NaOH 2) OH 1) SOCI 2, py 2) NaOEt 3) Br2, H₂O 3) OH 1) H2SO4 conc. 2) HBr, ROOR 3) KOtBu 4) OH 1) TsCl, py 2) NaOEt 3) 03 4) DMSarrow_forwardWhich of the following rings has the least strain in its most stableconformation?A. Cyclobutane; B. Cyclopentane; C. Cyclohexane; D. Cycloheptane;E. Cyclooctanearrow_forward
- The number of different carbon skeletons that have a main chain of 9carbons and an ethyl branch isA 3; B. 4; C. 5; D. 6; E. 7arrow_forwardQ5: Classify the following pair of molecules as constitutional isomers, enantiomers, diastereomers, the same molecule, or completely different molecules. Br O CI Br OH OH 111 Br .!!!/Br F OH and ...m Br Br OH CI Br OH ་་་་་" ། ་arrow_forwardConsidering only rotation around the 1-2 bond, how many differentstaggered conformations are there of 1,2-dibromo-1,2-dichloropropane?A: 2; B. 3; C. 4; D. 6; E. more than 6.arrow_forward
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