Check the box under each compound that exists as a pair of mirror-image twins. If none of them do, check the noneabove box under the table.OHCH3-CH-CH2-CH-CH3OHCH3 CH2 CH CH2OHCH30OHHO—CH—CH,—CH—OHOHCH3OHCH3 C-CH2-CH-CH3OHnone of the aboveExplanationCheckOX

It is the third compound (the one checked below):In chemistry, mirror-image twins, also known as…

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Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.71P

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I have the following data from an NMR scan. Five peaks; a doublet at about 0.8ppm (6H) a small single septet at about 1.5 ppm (1H), a triplet at 1.6 ppm (2H(, a singlet at about 2.1 ppm (3H), a triplet at about 4.4 ppm (2H). The molecular formula is C7H14O2. I calculated a degree of unsaturation of 1. I have tentatively identified the compound as methyl-4-methylbutanoate. I would appreciate any comments you care to make. Thank you.
Rank the following groups in order of decreasing priority. a. – COOH, – H, – NH2, – OH b. – H, – CH3, – Cl, – CH2CI c. -CH2CH3, -CH3, -H, -CH(CH3)2 d. – CH = CH2, – CH3, – C ≡ CH, – H
Assign relative priorities to each set of substituents: a. -CH2CH2CH3 -CH(CH3)2 -CH = CH2 -CH3 b. - CH2NH2 -NH2 - OH -CH2OH c. -C(=O)CH3 - CH =CH2 -Cl -C=N
An IR spectra show C—H peaks in the functional group region at values 2990 and 2890 cm^-1, but does not show any C—H peaks above 3000 cm^-1. What can be concluded about this compound? This compound only contains H’s bonded to sp3 carbons. This compound only contains H’s bonded to sp2 carbons. This compound only contains H’s bonded to sp carbons. This compound only contains H’s bonded to sp and sp2 carbons.
Considering R-S Convention Rules for naming enantiomers, which of the following groups will have lowest priority? Atomic Numbers: H=1, C=6, O=8, Br=35 options: -CH2-OH –CH2-CH2-Br –CH(CH3)2 –CH2-CH2OH –CH=CH2
(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).
First calculate r value of each then draw all possible structural and stereochemical isomers. Include enols and enamines and any e and z isomers. -C3H4O -C3H6O -C4H8O -C4H9N
Which one of these pair has a more inductive effect? 1. CH3CH2OH or CH3CH2OCH3 2.CH3CH2CH2CH2Cl or CH3CH2CH3CHCH2Cl
Convert each compound to hex-1-yne, HC=CCH2CH2CH2CH3.
Rank the compound in order of increasing stability and explain why.1. (E)-3-Methyl-2-pentene2. 3-Methyl-1-pentene3.2-ethylbut-1-ene
Draw a Newman projection looking down the C1-C2 bond of 1-chloro-2-methylcyclohexane in such a way that the two substituents are gauche to each other. Then draw another Newman projection in which the two substituents are anti to each other.
What is each compound’s systematic name? 1. (CH3)3CCH2CH2CH2CH(CH3)2 2. BrCH2CH2CH2CH2CH2NHCH2CH3 3.(CH3CH2)4C 4.CH3OCH2CH2CH2OCH3

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Check the box under each compound that exists as a pair of mirror-image twins. If none of them do, check the none above box under the table. OH CH3-CH-CH2-CH-CH3 OH CH3 CH2 CH CH2OH CH3 0 OH HO—CH—CH,—CH—OH OH CH3 OH CH3 C-CH2-CH-CH3 OH none of the above Explanation Check O X