2) Of the following alcohol, a) locate the chirality center, b) classify as 1°,2, or 3°,)...
7. Locate the chirality center(s) in the following compound. ГОН
Classify the structure below by Configuration, Family, Backbone, and # of Chirality Centers: CH2OH Н. -OH CH OH OL, triose, aldose, o OL, tetrose, ketose, 1 D, tetrose, ketose, 1 D, triose, aldose, o The product formed by the following reaction sequence is 1) HNOZ/H2SO4 2) C12, AICI: 3) Fe, HCI 4) NaNO,, HC1 5) KCN Identify the best method to prepare 5,5-dimethylhex-2-ene? CH2CH2CH2CH=PPhz + (CH3),C=0 OCH2CH=PPh: + (CH3)3CCH=0 O(CH3)3CCH2CH=PPhz + CH2CH=0 OCH3CH,CH=PPhz + (CH2CH2)2C=0
Classify each alcohol as 1º, 2º, or 3º. a. CH3CH2CH2OH 2° alcohol b. (CH3CH2)3COH ( 3° alcohol OH c. [ ( 1° alcohol A
draw the product when the alcohol is dehydrated with
h2so4
value: 10.00 points 3 attempts left Check my work Click the "draw structure" button to launch the drawing utility. Draw the product formed when the alcohol is dehydrated with H2SO4- OH CHCH2CH3 інсну. edit structure ..
(Hint, draw it out....) 1-Methylcyclopentanol is classified as A) a primary alcohol B) a secondary alcohol C) a tertiary alcohol D) a phenol E) an enol 2. (1 pt) Provide the IUPAC name for the following compound. OH 3. (1 pt) Provide the major organic product of the reaction below. 1, NaH HCM,CH 2 CHỊCH CHI
1. Assign R or S configuration to each indicated chirality center (carbon A and B) in the following molecule (vitamin C). Which of the following assignments is correct? но OH HO H. a. carbon A (R); carbon B (S) b. carbon A (R); carbon B (R) c. carbon A (S); carbon B (R) d. carbon A (S); carbon B (S) 2. Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How many chirality centers does erythronolide B have?...
Alkenes can be converted to alcohols by hydroboration-oxidation.
Draw the structure of the alcohol(s) formed in the following
reaction sequence. If applicable, draw hydrogen at a chirality
center and use wedge-and-dash bonds to designate the
stereochemistry.
Select all that apply: The alcohol product(s) of the reaction is
characterized as being
_____ R,R
_____ R,S (and/or S,R)
_____ S,S
_____ achiral
_____ racemic
_____ diastereomers
_____ R
_____ S
Classify the structure below by Configuration, Family, Backbone, and # of Chirality Centers: CHO H OH HO H CH2OH D, triose. ketose, 1 D, tetrose, aldose, 2 L, tetrose, aldose, 2 L, triose, ketose, 1
2. Assign Ror Sfor each chirality center in the following molecules 3 point OF Is the compound b chiral or achiral? Explain (4 points) Chiral 3. Which one of the following hydrogens is the most reactive when the compound reacts with Bry/hu? Pick your answer and explain. (4 points) А в р WCH, H нсен 4. A secondary hydrogen is indicated at which position in the structure above? (2 points)
3) Draw the disaccharide that is formed when the following two mon joined by a B (1-3) glycosidic linkage. (2 pts) two monosaccharides are CH₂OH онон - он снон, 9 w OH 3 OH CH, OH OH OH OR 0 Y 4) Consider the disaccharide sophorose, a product of the caramelization of glucose, answer the following questions: CH,OH Мон OH ОН a) Classify the glycosidic linkage as a or B, and use the numbers to designate its location. (1 pt)...