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Question 26 5 pts Assign the absolute configuration to the carbohydrate depicted. Select all that apply....
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for each. Also write whether the molecule is chiral, achiral, or meso (3 pts each) H CH2OH b. c. tch Br Сн, 3. Name the following compounds (2 pts each) Br b.
Testbank, Question 114 Assign the following stereocenter as having the R or s absolute configuration. HO+H : O There are no stereocenter in this compound
designate the R/S configuration for any chiral centers
нсн, но, сня H.CH, H, CH3 Но, | | H NH20 Кн 23, HC NHA 24. нсн, нсна H CH3 нон Дн 26 но сн, .. .CH OH нд но со Р o . 28 ноги нас < HO 29. Но LOH не 30.
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br CH, Br CHECH, H CH2CH3 CH2CH3 CH, CH, -CHE OH H CH=CH2 H3CH2 HY CH(CH3)2 CH 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers Identical d Meso Compounds
5. For the structure, CHO НЕОН H+OH CH,OH (a) Draw all the stereoisomers. (b) Label structure as chiral or achiral. (c) Assign each chiral center as (R) or (S). (d) Give the relationships between the stereoisomers (enantiome (e) Label any meso compounds. 6. Give the structures of the following compounds. Classify the com primary, secondary, or tertiary halide if possible. (a) Sec-butyl chloride (b) Isobutyl bromide (c) Chloroform (d) Tert-pentyl iodide (c) 2,2,2-trichloroethanol (f) Methylene chloride
4. (26 points) Identify each chiral carbon in the molecules below with an asterisk (*) and assign R or s absolute configuration to each chiral carbon. Then, state (in the box provided) whether the molecules are enantiomers, identical, diastereomers, or not related. Hint: if it looks like a Fischer projection then it is a Fischer projection. ...1111 O піон аnd and .Ley O Era o C CHO CH,OH C. H oH and OHCH IH Сн,он
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
Can yall please check solutions, I am not sure if they are
correct thanks
СНО ОН Br НО Н NC Compound A Compound B Compound C Compound D СНО Br F CHO HS CHз Compound H Compound E Compound F Compound G Determine if the stereochemistry of each of the above O= True If the R isomer of a molecule has an optical rotation of + 25.7° then the S isomer of the molecule will have an optical rotation of...
Could u please help me with numbers 1, 8, 9, 2, 3, 4 and also
the one under 4 numbered 1. thanks in advance
1. Which of the Fischer projections correctly depicts the following compound? To do this problem, first determine R/ configuration of the compound in question, then do same for a, b, c, d. There could be an easier way. нон ң он CHCH но н @ CH (6) CH (©) CH (@ CH нон нонн ньоннон но...