With explanation, please Draw the enantiomer of the following compound.
7. Draw the enantiomer of the following compound.
Be sure to answer all parts. Draw the enantiomer and a diastereomer for the following compound. (I got the diastereomer wrong) Be sure to answer all parts. Draw the enantiomer and a diastereomer for the following compound. HO HO OH OH OH OH edit structure.. edit structure.. 2 Enantiomer Diastereomer Feedback When drawing an enantiomer, be sure you have drawn a non- superimnposable mirror image When drawing a diastereomer, check to see that one stereogenic center is different from the...
7.(a) Draw and label (a) the enantiomer and 6) compound. (4 points) me enantiomer and (b) a s of diaststomers of the following (b) Will a 50:50 mix of the enantiomers be optically active (rotate plane polarized light). Explain the reason for your answer (3 points) b) Will a 50:50 mix of the two structures you drew in (b) be optically active (rotate plane polarized light). Explain the reason for your answer (3 points) 8. Assign the chiral center as...
1(12 pt). Draw the Fischer projection of the enantiomer and one diastereomer of the compound shown below and provide the name of the enantiomer and diastereomer: -CH2CH3 H3C- ci CH2CH2CH2CH3 Structure of enantiomer Structure of diastereomer Name of enantiomer Name of diastereomer
Draw one enantiomer and one diastereomer of your compound if applicable. If not applicable, state why not. НО НО
3. Provide an explanation for the results shown below involving monosubstituted cyclohexanes. 4. The compound below has an enantiomer despite having no chiral centers. Draw its enantiomer and explain why this molecule is chiral. i know i have the enantiomer right but im not sure about the explanation. thank you! 3) Provide an explanation for the results shown below involving monosubstituted cyclohexanes at 25°C. (6 points) [equatorial Keq axial Substituent 1 -H 18 -CH -CH2CH -CH(CH) -C(CHs)s 21 35 4800...
please help (9 points) Given the 2R, JS isomer below, draw the other enantiomer and the two diastereomers of this compound and indicate the stereochemistry of each. CH НО -н HB CH Enantiomer 1 Enantiomer 2 Diastereomer1 Diasteromer 2 Stereochem 2R.53 (12 points) Write the complete name or structure of each of the molecules below on the line provided. No stereochemistry is needed unless indicated NO C(CH3) Br=CHCHCH,CH,CH c). cis-3-chloro-4-methyl-3-hexene d). 4-isopropyl-2-heptene
please help 14. The alcohol below was optically pure (ie, one enantiomer). After treating with dilute H2SO, in water the optical rotation chana as shown in the graph. NMR and IR spectra confirm that the compound after this treatment had the same constitution as before Explain this observation. Draw a mechanism to support your explanation and draw all reaction products. OH optical rotation HC time
If possible, draw the structure of the enantiomer of the molecule shown below. CH3 НАС Draw the enantiomer of the given molecule. If there is no enantiomer, draw the given molecule in the space provided. 2 . ⓇH1200 mm Marvin JS ChemAxon 1 oooooood