Steps and explanationn please. Give the structure corresponding to each name.a. 3-chloro-2-methylhexaneb. 4-ethyl-5-iodo-2,2-dimethyloctanec. cis-1,3-dichlorocyclopentaned. 1,1,3-tribromocyclohexanee. 6-ethyl-3-iodo-3,5-dimethylnonanef. (R)-1-fluoro-2,6,6-trimethylnonane

Answered: Image /qna-images/answer/06f872fd-0596-46f0-b16e-c71df359b3fe.jpg

Answered: Give the structure corresponding to…

World of Chemistry, 3rd edition

3rd Edition

ISBN:9781133109655

Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Chapter20: Organic Chemistry

Section: Chapter Questions

Problem 4STP

See similar textbooks

Similar questions

8. What is the IUPAC name of CHCH, CH, CH3-CH-O-CH, CH; Da. 1-ethoxy-1-methylbutane Ob. 2-ethoxypentane O c. 1-methoxyhexane Od. 2-ethoxy-2-n-propylethane
Compound III (in the provided image) is I. CH3-CH2-C = C-CH3 III. CH3-CH-C=C-CH-CH3 O a. 2-ethyl-5-methyl-3-heptyne O b. 2,5-dimethyl-3-heptyne O c. 2,5-dimethyl-3-hexyne O d. 2-ethyl-5-methyl-3-hexyne CH3 CH2-CH3 II. CH2=CH-CH2-CH-CH3 CH3
Which structure below represents 4-methylpent-2-ene? a. CH3-CH2-CH2-CH2-C=CH2 O b. CH3-CH2-C=CH-CH3 O c. O d. CH2-CH3 CH3 CH3-CH-CH=CH-CH3 CH3 CH3-CH2-CH-CH=CH2 CH, CH3
CH3 2. Give the structure corresponding to each IUPAC name. a. 3-ethyl-3-methylhexane b. 2-ethyl-1-methyl-3-propylcyclopentane c. 3-methylbutane d. 1-ethyl-2,3-dimethylcyclopentane e. 1,5-dimethylcyclohexane
Name each carbon chains.
9. Select the correct IUPAC name for : H,C- .CH, A. 1,4-dimethylcyclopentane. B. 1,3-dimethylcyclopentane. C. 2,5-dimethylcyclopentane. D. 2,3-dimethylcyclopentane. Agoula E. 2,4-dimethylcyclopentane. nob
Draw the structure corresponding to each IUPAC name. a.3-ethyl-2-methylhexane b. sec-butylcyclopentane c.4-isopropyl-2,4,5-trimethylundecane d.cyclobutylcycloheptane e.3-ethyl-1,1-dimethylcyclohexane f. 4-butyl-1,1-diethylcyclooctane g.6-isopropyl-2,3-dimethyldodecane h. 2,2,6,6,7-pentamethyloctane i. cis-1-ethyl-3-methylcyclopentane j. trans-1-tert-butyl-4-ethylcyclohexane
Please do the following question step by step . A. 1,3- cyclopentadiene + CH2 = CH – COOH B. 2-methyl-1,3-pentadiene + trans – CH3- CH = CH - COOH
Reagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
What is the preferred IUPAC name of the alkene shown in Figure below? CH3 CH3 CH3 `CH-CH3 A. 1-ethyl-2,4,5-trimethylcyclohexene B. 2-ethyl-1,4,5-trimethylcyclohexene C. 2-ethyl-1,4,5-trimethylcyclohex-1-ene D. 4-ethyl-1,2,5-trimethylcyclohexene
12. Write structural formulas for the following alkene names. a. hept-2-ene b. hex-2-ene 6,7-dimethyloct-1-ene d. 2,4-dimethyloct-4-ene с. 3-ethylnon-2-ene е.
5. What is the IUPAC name for the structure below? ОН A. 3-ethyl-4-methyl-2-hexanol B. 2-ethyl-1,3-dimethyl-1-heptanol C. 4-ethyl-3,5-dimethyl-5-hexanol D. (1-hydroxyethyl)-3-methylhexane

SEE MORE QUESTIONS

Recommended textbooks for you

World of Chemistry, 3rd edition

Chemistry

ISBN:

9781133109655

Author:

Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Publisher:

Brooks / Cole / Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

World of Chemistry, 3rd edition

Chemistry

ISBN:

9781133109655

Author:

Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste

Publisher:

Brooks / Cole / Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

Give the structure corresponding to each name. a. 3-chloro-2-methylhexane b. 4-ethyl-5-iodo-2,2-dimethyloctane c. cis-1,3-dichlorocyclopentane d. 1,1,3-tribromocyclohexane e. 6-ethyl-3-iodo-3,5-dimethylnonane f. (R)-1-fluoro-2,6,6-trimethylnonane