(e) (Z)-3-Chloro-2-butene .Numbering must begin at the end of the chain Correct name is (Z)-2-chloro-2-butene double bond occurs at an equal distance from either end of the longest chain, choose the name that gives the lower substituent group(s) at the first point of difference. (f) 5,6-Dichlorocyclohexene nearer the double bond. When: numbe Correct name is 4,5-dichlorocyclohexene Substituted cycloalkenes are numbered in the way that gives the carbon atoms of the double bond the 1 and 2 positions and that also gives the substituent groups the lower ✓numbers at the first point of difference.

(e) (Z)-3-Chloro-2-butene .Numbering must begin at the end of the chain Correct name is (Z)-2-chloro-2-butene double bond occurs at an equal distance from either end of the longest chain, choose the name that gives the lower substituent group(s) at the first point of difference. (f) 5,6-Dichlorocyclohexene nearer the double bond. When: numbe Correct name is 4,5-dichlorocyclohexene Substituted cycloalkenes are numbered in the way that gives the carbon atoms of the double bond the 1 and 2 positions and that also gives the substituent groups the lower ✓numbers at the first point of difference.

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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6. Which of the following alcohol/s would give a positive triiodomethane reaction? Indicate YES or NO on the boxes provided below the structure OH OH CH3(CH,);-CH,OH CH, —С—н (a) (b) (c)
The following names are all incorrect. Draw the structure represented by the incorrectname (or a consistent structure if the name is ambiguous), and give your drawing thecorrect name.(a) cis-dimethylpent-2-ene (b) 3-vinylhex-4-ene(c) 2-methylcyclopentene (d) 6-chlorocyclohexadiene(e) 2,5-dimethylcyclohexene (f) cis-2,5-dibromo-3-ethylpent-2-ene
Determine which compounds show cis-trans isomerism. Draw and label the isomers, using both the cis-trans and E-Znomenclatures where applicable.(a) pent-1-ene (b) pent-2-ene(c) hex-3-ene (d) 1,1-dibromopropene(e) 1,2-dibromopropene (f) 1-bromo-1-chlorohexa-1,3-diene
Write structural formulas for the following compounds (includes both old- and new-style names). (h) (E)-6-ethyloct-2-en-4-yne (i) 1,4-heptadiyne (j) vinylacetylene (k) (S)-3-methyl-1-penten-4-yne
For each alkane, which mono brominated derivatives could you form in good yield by free-radical bromination?(a) cyclopentane (b) methylcyclopentane(c) 2-methylpentane (d) 2,2,3,3-tetramethylbutane
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2. Explain why each of the following names is incorrect: (a) 2,2-Dimethyl-6-ethylheptane (c) 3-Ethyl-4,4-dimethylhexane (e) 2-lsopropyl-4-methylheptane (b) 4-Ethyl-5,5-dimethylpentane (d) 5,5,6-Trimethyloctane
Specify reagents suitable for converting 3-ethyl-2-pentene to each of the following: (a) 2,3-Dibromo-3-ethylpentane (b) 3-Chloro-3-ethylpentane (c) 3-Ethyl-3-pentanol (d) 3-Ethyl-2-pentanol (e) 2,3-Epoxy-3-ethylpentane (f) 3-Ethylpentane
Give IUPAC names for the following substances (red = 0, blue = N). (a) ** (b)
Write structural formulas for the following compounds (includes both old- and new-style names) (d) cyclohexylacetylene (e) 5-methyl-3-octyne (f) trans-3,5-dibromocyclodecyne (g) 5,5-dibromo-4-phenylcyclooct-1-yne
(a) Draw a three-dimensional line structure of (5R,6Z)-6,7-dichloro-5-hydroxynon-6-enal. Place the aldehyde group on the right-hand side of your drawing.(b) Give the Cahn-Ingold-Prelog priority order of the four groups (-OH, -H, -(CH2)3CHO, -C4H5Cl2) at the C5 stereocentre (Highest 1 > 2 > 3 > 4 Lowest).
Indicate the letter of the correct answer and kindly briefly justify the letter of answer. Cyclohexene undergoes hydrobromination. Which of these is a possible product? (A) Bromocyclohexane (B) All of these (C) Trans 1,2-dibromocyclohexane (D) Cis 1,2-dibromocyclohexane