Take a look at the following molecule, and then answer the questions in the table below it. (You can click the other tab to see the molecule without the coloredregions.)with colored regionplain0=CH2-0-C-(CH2)16-CH3=0CH-O-C (CH2)7-CH=CH-(CH2)5-CH3DCH3| +OMPLOCH3-N-CH2-CH2-0-P-O-CH2BCH3ATry again *000Ar8 0?

Answered: Image /qna-images/answer/7efc737c-7c68-4249-a06f-e65a073d6fe4.jpg

Answered: Take a look at the following molecule,…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 21E

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6. For each pair of compounds below determine whether they represent the same molecule, enantiomers, or diastereomers. CH H₂N H CH J OllinO 2||2 COOH C OH CH₂ OH NH₂ CH, COOH CH3 HO H₂N CH₂4 CH CCC COOH OH NH₂ NIIIIIC CH₂ H CH3 CH3 H₂N HO H₂N COOH CH OH 5- O J CH3 COOH O H CH₂ H COOH HO CH CH₂4 HOOC COOH ........ OH JCC H NH₂ NH₂ CH₂
Draw a structural formula of the SR configuration of the compound shown below.
Question 3: Please state whether each of the following molecules is chiral or achiral. If you believe it is achiral, indicate the element of symmetry [plane of symmetry or center of inversion] responsible for the achirality. H3C H3C |H3C OH Br Br -H H CI Br но H Н CI CI CI ОН НН ОН H CI ОН ОН Br- Br H3C. .H неи Н' С2Н5 Н CI CI Br >
2. From the molecules below, determine the relationship between each pair (a-b, a-c, a-d, etc.): identical, constitutional isomers, enantiomers, diastereomers. In this problem, conformational isomers are considered identical, PUCH H HOCH an e OF CH 學 HOCH。 HOCH CH H OH 10- h H d. E HO CH "OH CH₂CH PHON 美 FOH H -OH
The following molecules are: Hint: Build models and relate structures or perform a configurational assignment for each asymmetric center. They are identical if they are both "S" configured. They are identical if they are both "R" configured. They are enantiomers if one is "R" configured and the other is "S" configured.
What is the relationship (same, enantiomers, or diastereomers) between the following two molecules? You should find the absolute configuration at the stereo center to answer this question. H CH... HS CH₂OH HOH₂C H SH
Organic chemistry
One of the isomers of 1,2,3,4,5,6-hexahydroxycyclohexane, called myo-Inositol, acts as a growth factor in both animals and microorganisms. Draw the most stable chair conformation of myo-Inositol (Note: account the wedge and dash projection). Draw the most stable cis-trans stereoisomer of myo-Inositol. OH HO ОН HO "OH ОН
For each of the following pairs of molecules, classify them as either: enantiomers, diastereomers, identical compounds, or constitutional isomers.
Draw a structural formula of the RR and RS configuration of the compounds shown below.
For the following molecules, draw all possible stereoisomers using line-angle formulas with wedge/dash notation. Label the stereocenters as R or S. Indicate which ones are enantiomers and which ones are diastereomers. (Remember: there are 2 stereoisomers possible for a molecule with n chiral centers) (A) (B) (C) (1 chiral center) Br OH (2 chiral centers) CI OH CH3 (3 chiral centers)
Determine: The number and placement of the carbon chirality centers, if any. If this structure can have an enantiomer, why? What is the configuration of the highlighted carbon and how did you determine that?

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