Q: (a) Describe the molecular geometry expected for 1,2,3-butatriene (H2C=C=C=CH2). (b) Two…
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Q: Assign the configuration to each asymmetric carbon as R or S. NO2 (b) NO2 (c) (d) OCH3 (a) Br
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Q: CH3 .CH3 What is the name of the following?
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Q: III. Give IUPAC names for the following cycloalkanes: CH2CH3 a) CH3 b) CH2CH2CH3 c) d) ČH3 CH3 Br
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Q: Draw the cis and trans of these compounds, if cis-trans isomers do not exist, write none. 1-hexene…
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Q: b) a) CH3 CH3 CH2CH3 CH3 •CH3 H3CH2C. CH3
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Q: 2. Which of the following compounds exhibit cis/trans isomerism? Explain why. Draw the Cis and trans…
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Q: Draw all possible configurational isomers for the compound shown below. HOHOHO H3C-C-C-C-CH3 H H…
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Q: Draw structural formulas for the following compound Q}.rans-1-Bromo-3-isopropylcyclohexane
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Q: Which of the following organic compounds is in the cis isomer for CH3CH₂CH=CHCH₂? 0 a) b) I H₂CH₂C…
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Q: Which of the following is a constitutional isomer of heptane? CH3 H3C. CH3 CH3 H3C CH3 CH3 H2C- CH3…
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Q: Which of the following does not represent 2-methylbutane? H₂C-CH₂ CH3 CH₂ CH₂ CH₂ CH (CH₂)₂ 2 C B D
A: Given,
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Q: Consider the sawhorse representations below labeled A and B and answer the question that follows.…
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Q: NH2 C' HC C-c=C- H2C-HC CI H2 HC
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Q: CH3 CH3 H-C CH CH3 H3C This compound has how many chiral carbons? 3.
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Q: Draw a structural formula of the R configuration of the compound shown below. ÇH2NH2 CH2OH
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Q: c)Conformational isomer is the different spatial arrangement of the atom that resulted from rotation…
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Q: Which of the following can exist as cis-trans isomers? O a) cyclohexane b) methylcyclohexane O c)…
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Q: What is the closed formula of the following structure? но. HO. NH2 OC15H20N205 OC13H16N205…
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Q: OH H;CH2C H. C%3C CH2CH2CI CH3 CIH,CH2C F
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Q: Consider the cyclohexane structure below. Select which substituents (labeled A, B, and C) will be in…
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Q: Draw the compound: 1. Methylbutanoate Systematic name of the compounds: 2. CH3C=CC=CCHCH2CHC=CH…
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Q: Draw all the possible noncyclic structural isomers of C5H10. Name each compound.
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Q: Consider the substituted cyclohexane shown in the ball-and-stick model. (See attached) Are the…
A: The substituents on C2 and C4 cis to eachother or trans to eachother has to be given.
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- Draw a structural formula of the SS configuration of the compound shown below. CH2F HO2C • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.Draw a structural formula of the S configuration of the compound shown below. • Use the wedge /hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • Ifa group is achiral, do not use wedged or hashed bonds on it. CH3 CH3 CH;CHCHCN CH,CH,CH,CHCH,CH, CH2NH2 Draw a structural formula of the RS configuration of the compound shown below. Use the wedge /hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. ÇIDraw a structural formula of the S configuration of the compound shown below. OH -CHCO2H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.
- Draw a structural formula of the SS configuration of the compound shown below. S OH S CH3 CH₂CH3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.Draw a structural formula of the S configuration of the compound shown below. CH3 CH,CHCHCN | CH;NH2 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.Draw a structural formula of the R configuration of the compound shown below. ÇNH₂ CN • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. #[ ] در ?
- Draw a structural formula of the SR configuration of the compound shown below. OH • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.Draw a structural formula of the S configuration of the compound shown below. CH3 CO2H Ibuprofen • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. opy asteDraw a structural formula of the SR configuration of the compound shown below. HO CH3 S -NHCH3 R H3C ephedrine • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. * #[ ] در ?
- Draw a structural formula of the R configuration of the compound shown below. -OH Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it.Draw a structural formula of the S configuration of the compound shown below. CH₂CI [Referer • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. •If a group is achiral, do not use wedged or hashed bonds on it. n ? ChemDoodleDraw a formula for the lowest molecular weight compound that contains C, H, and possibly O, N or 5, is a chiral compound, contains ONLY one functional group, and is a sulfide. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. Alkene or alkyne groups are considered to be functional groups. 98 4 - /IP ChemDoodle