what do the following diastereomers/enabtiomers of these molecules look like? b) Draw ONE diastereomer of this...
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. Draw the enantiomer and one of the diastereome respective order. one of the diastereomers of the following molecule in the OH 20- 0- SH B H- - C- OH CH OH 8. What is the maximum number of hydrogen atoms that can be attached to 97,642 carbon atoms? 9. What is the relationship between the two molecules? CH OH CH2OH H-C-OH HO—• —H H-¢-OH HO–H CH,OH CH,OH
LS 197 Homework Set 8: Name: 4) Draw the enantiomer of the following molecules: 5) Draw the enantiomer and a diastereomer of the following molecule: OOH 오인 OH HOT оно L-tartaric acid 6) Predict the products of the following reactions and identify the type of reaction: OH HO HCI Catalyst ZI Sucrose CH OH O 0 CH,OH Sucrase enzyme catalyst в усн он OH Fructose Glucose OH Sucrase is an enzyme that breaks sucrose into glucose and fructose
003 2) draw the enantiomer and a diastereomer of ribose shown below (6 point) OH HO HO OH Hou 3) Draw all the hydrogen bonds that one ethanol molecule can form with water molecules (6 ponit)
Question 20 HzC CH Which of the three molecules below is a diastereomer of the following molecule? " Но у он Hн нсон нс сни нус, CH Ноун н "Н HYPOH HCH но ОН НО II III Н A both I and II Ов. І oc there are no diastereomers СЕ III
DUBU Ugraded 1) Draw the enantiomer and a diastereomer of the following Fischer projection in the boxes below Your answers should be in wedge/dash notation (2 points) Original molecule Enantiomer Diastereomer OOH -OH C-Me SH Merci 2) Provide the full IUPAC name for the following molecule (2 point): undecane 3-bromo 4,5-ethyl 6-methyl 8-ethylene Molecule: 9-11-methylethul) Name 3) Use your knowledge of pka's to rank the following from least basic (1) to most basic (5)? (1 point)
3. a. Consider molecule A below. Draw its enantiomer in box B and two unique diastereomers in boxes C and D. Assign each stereocenter Ror S, and each alkene E or Z. 3b. What is the relationship between B and C? А B, enantiomer of A 3b. What is the relationship between B and D? Br 3c. What is the relationship between C and D? 3d. The specific rotation of A is -7.38°, what are the specific rotations of B,...
diastereomer 8. (1 pt.) Identify the specific type of relationship between each of the following pairs of molecules (i.e., either the same, constitutional isomers, enantiomers, diastereomers, conformers or unrelated). Br HOM Br Br a) b) d) H OH CL c HO- -Hi Be H- OH HO H e) f)
7,8 1.1 pt) A. Designate the content e configuration of each stereoisomer for each molecule. in the phenstructures as Ror 5 B. Draw indicated OH enantiomer diastereomer 8.1 p.) identify the specific type of relationship between each of the following pairs of molecules (le, either the same, constitutional isomers, enantiomers, diastereomers, conformers or unrelated)
Create model Epibatidine | A) label euch stereo center, as Rors B) Draw a diastereomer of epibutidine. | C.) Draw an enantiomer of epiputidine. | D) Do you expect the enantiomer to have analgesic properties. Explain rearning Cu Hiz CIN2