If you're going to write it down, please write it clearly Draw the structures (expanded) of the following compounds:g. 1-butyl-4-ethylbenzeneh. 1-chloro-2-(2-chloropropyl)benzenei. 1-chloro-2,4-dimethylbenzenej. o-phenylphenol

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Answered: Draw the structures (expanded) of the…

Chemistry: Matter and Change

1st Edition

ISBN:9780078746376

Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom

Publisher:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom

Chapter21: Hydrocarbons

Section: Chapter Questions

Problem 91A

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2. Consider the following organic molecules A-H. Many of them are natural products isolated from Nature. Please answer the following questions by writing the Letter pertaining to each molecule next to the question. -N- H;C "CO,H N. Но CH2 ČH3 B strychnine (a plant alkaloid) hirsutic acid A nepetalactone (essence of cutnip) (a fimgul metabolito) H- H. I CH,0 E helminthosporal (a imgal toxu) D progesterone F cantharidin (a progestin hommone) (am insect vesicant) Br NO2 Br CI G untenine C (E)-1,6-dibromo-2,7-dichloro-3,7-dimethyloct-3-ene (fom red algae) (4 sponge metabolite)
3. Complete the chemical equations for the following reactions. Draw the structure (condensed structural formulas) for the dominant product and write the names of the reactants and products (organic compounds only.) d) CHy Name reactant: Name product: e) CH=C-CH + 2 HBr 4-Cて。 Name reactant: Name product:
2) Please complete the following syntheses A) Propene to 2-methyl-pent-2-ene B) pentan-2-amine to 3-bromopentane
5. Nomenclature following molecules. a. 2. Cu ts). Draw the appropriate structure and provide an IUPAC name for the 3-(N-methylamino)propanoic acid b. m 'N H
4- Choose the correct reactants required to synthesize the following molecule. H3CO OCH 3 A. Acetone and methanal B. Acetone and methanol C. Formaldehyde and propanal D. Formaldehyde and propanol 5- What is the IUPAC name of the following compound? CI A. 6-Chloro-4-ethoxy-1-octanal B. 6-Chloro-4-ethoxyoctanal C. 6-Chloro-4-ethoxycyclooctanal D. 4-Ethoxy-6-chlorooctanal - What is the IUPAC name of the following compound? 0 Br. Br Cl A. 2,6-Dibromo-3-chloro-5,5-dimethylhexanone B. 2,6-Dibromo-3-chloro-5,5-dimethylcyclohexanone C. 2,6-Dibromo-5-chloro-3,3-dimethylhexanone D. 2,6-Dibromo-5-chloro-3,3-dimethylcyclohexanone
B. Draw structures corresponding to the following names. 1. 3-methylbutanal 7. 4-chloro-2-pentanone 2. o-hydroxybenzoic acid 8. phenylacetaldehyde 3. 3-chloro-4-cyanopentanoic acid 9. cis-3-tert-butylcyclohexanecarbaldehyde 4. 3-methyl-3-butenal 10. 2-(1-chloroethyl)-5-methylheptanal 5. 2,3-dimethylhexanoic acid 11. trans-1,2-cyclobutanedicarboxylic acid 6. 2-hexen-4-ynoic acid 12. heptanedioic acid
Draw 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 acid
Define two methods can be used to convert cyclohexanone into alkene B (methylene-cyclohexane) ?
2- 1- Pentyne fiome brome propan- Qe Prefare The following compounds 1. Iso propyl Alcohol from Proelene 3. Acetaldehyde fram Acetylene- y. 1,2- Di bromo Propan from Propene. * Iso butyl chloride from Isebutan .
4. Draw the following compounds a. 1-chloro-4-ethyl-3-methylnonane [ Gatusofom gnit b. 4-methyl-2-pentyne Job i anticas) enod totall xbacd bigin i emoczopertori c. 1-bromo3-methylbutane d. 4-ethyl-3-fluoro-1-hexene
Draw structures for each of the following carbonylcompounds.a. 2,2-dichloro-3-pentanoneb. 4-methylpentanalc. isopropyl hexanoated. octanoamidee. 3-fluoro-2-methylbutanoic acidf. cyclopentanalg. hexyl methanoate
1. 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-ethylheptane

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Draw the structures (expanded) of the following compounds: g. 1-butyl-4-ethylbenzene h. 1-chloro-2-(2-chloropropyl)benzene i. 1-chloro-2,4-dimethylbenzene j. o-phenylphenol