Homework Answers
Note: a and b both questions are same.
1)
a) left side of group in fischer projection are writing upper side in Haworth projection & right side of group in fischer projection are written down side in Haworth projection.
Hence none of the given options A,B,C & D are correct.
But
The correct Haworth projection is shown in the image.
1-c) correct option is (C).
Because we already know, that upper side group in Haworth projection are written left in Fischer projection & down side group in Haworth projection are written right side in Fischer projection.
Further detailed explanation are provided in the image.
Hence option (C) is correct.
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1a. For this question, select the LETTER of the structure that corresponds to the given Fischer...
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Identify each of the disaccharides as a reducing sugar or a nonreducing sugar. Reducing sugar Nonreducing sugar CH, OH он CH OH CH OH OHN Кон ни и н IVO 5 5-т ен,он он н CH OH нон сн,он Сн,онн Үн нуконн Ин но он снон Кон вън онусн,он н он он н н Answer Bank
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rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
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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....
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не —...
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
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Answer for 1a and 1b
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Spring 2020 E. Carbohydrates Part 1: In the box, draw the Fischer projection (linear conformation) that corresponds to the Haworth projection sugar given below. Note: This sugar is a ketose. (6 pts) СН2 она to 2 но - н 3 н он ч CH,OH Р +он 5 ОН 5 Н НО а H снаби о Сн,он ОН Н Part 2: Draw the Haworth projection of the given monosaccharide as a 6-sided a-pyranose ring. (7 pts) Н. 0 / са он...
Identify each of the disaccharides as a reducing sugar or a nonreducing sugar. Reducing sugar Nonreducing sugar CH, OH он CH OH CH OH OHN Кон ни и н IVO 5 5-т ен,он он н CH OH нон сн,он Сн,онн Үн нуконн Ин но он снон Кон вън онусн,он н он он н н Answer Bank
SHORT ANSWER. Write the word or phrase that best completes each statement or answer the question. State whether each of these structures shown in the Hayworth projection is the a-or f-isomer. CH OH Кон он авлат 2) CH OH но но он не сH, - -0 он нон Кон на н он — алтанд Identify each Fischer projection as the D- or L-isomer. но НЕОН но -н Сн,ОН
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Which structure is a B-D-glucose and which is a ketose? If none, say NONE. CH2OH ни — он кон на Но Н ОН Іг? Конн ОН НОН oI-FI CH2OH Онон / Суон Hн CH2OH 0 он D Конн/ HOH нон
35. Enzymatic processing to break down glycogen into glucose occurs at: a. a reducing end. b. a non-reducing end. c. reducing and non-reducing ends simultaneously. d. branch points exclusively. 36. Which furanose is the B anomer of the monosaccharide given by the Fischer projection below? CH2OH 0= но о он a OH но о K он но, HOT о, -н он о. он Он KOH /он но TOH Нон но LOH HO но н но - он но -ОН -н...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
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....
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
Answer for 1a and 1b
1. Below are the cyclic and open-chain structures for glucose and fructose. (6 points total) а) Label each structure as glucose or fructose. (1 pt each, 4 pts) b) Glucose is a(n) and fructose is a(n). (ketose, aldose) (1 pt each, 2 pts) CH,OH -он HOCH ОН HOH н но/сн,он он OH H o=4 нон Но+н н+он н+он CH2OH CH2OH с=0 но-н нон н+он Сн,он
Spring 2020 E. Carbohydrates Part 1: In the box, draw the Fischer projection (linear conformation) that corresponds to the Haworth projection sugar given below. Note: This sugar is a ketose. (6 pts) СН2 она to 2 но - н 3 н он ч CH,OH Р +он 5 ОН 5 Н НО а H снаби о Сн,он ОН Н Part 2: Draw the Haworth projection of the given monosaccharide as a 6-sided a-pyranose ring. (7 pts) Н. 0 / са он...
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