3. (2 pts) Use the Fischer projections shown below to answer the following questions. Reference Sugar...
7. For the following monosaccharides, give the corresponding Fischer projection. CH OH —0 ОН CH,он Но —0 ОН НО У (он но У HO сно F 8. For the following monosaccharides, give one possible Haworth structure. CHO H- OH HOH Нонн — он нон CH OH CH OH от т т н-
Given the Fischer projection of the sup sugar, draw its Haworth projection (B-anomer only) Fischer Projection H Haworth Projection (B-anomer) CH, OH on CH OH 5. Identify the glycosidic linkages for the following disaccharides. Determine whether the disaccharides are reducing or non-reducing sugars. сон OH OH OH OH CHOH Снон не Он н Снон онон | CH, OH нон CH-OH
QUESTION 4 Which of the following Fischer projections corresponds to the compound shown below? НОН H,C, X Br CHz CH; CH3 сн; CH, НЕОН н—ОН НОЁН НОНН H-HBr Br-н H-Br BrEH Сн, сн, ён, CH, А) В) CH -
4.23,4.24 & 4.26 thank you 156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23 Draw the condensed structural formula for each of the following alkyl groups: a. propyl b. methyl 4.24 Give the correct name for each of the following substituents: a. CH CH - b. CH3CH,CHCH- c. I- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the following compounds: a....
ÇI-lagl- (2 pts) Use the Fischer projection shown below for the sugar D-altrose to draw a Haworth projection of the beta- 2. pyranose form of this sugar. но -Н H- OH H- OH OH H- CH-ОН 1
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
Draw the Fischer projections of the four aldotetroses. Draw the D-sugar on the left and its L-isomer directly to the right of it. Be sure you select the appropriate hydroxy group so that the bond carbon is connected to the oxygen bond. Draw D sugar 1 Draw L sugar 1 H H CH2OH Answer Bank CH2OH -OH Н но- Draw D sugar 2 Draw L sugar 2 H Answer Bank CH2OH CH-он он н Но- Draw D sugar 2 Draw...
Chem 1205 Recitation #10 Questions 3: Use the templates provided to draw the Haworth Projections for a- & B-anomers: HOH но -н но -н H- OH CH, OH HH tilt 'tip' structure over Rotate bottom carbon to put -OH at end Draw Haworth canomer B-anomer Question 4:Label the glycosidic linkages in the given disaccharides: сон - AM OHH CH 6-18 IVO
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...