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Q29.
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29. Statements: (1) Cellulose and amylose...
For each of the disaccharides or polysaccharides select from the response list the correct hydrolysis products....
For each of the disaccharides or polysaccharides select from the response list the correct hydrolysis products. Responses may be used more than once or need not be used at all. a) glucose only b) glucose and galactose c) glucose and fructose d) glucose and ribose 35. Sucrose 36. Lactose 37. Cellulose 38. Starch 39. Glycogen For each of the disaccharides or polysaccharides select from the response list the correct characterization of the type of glycosidic linkages present in the compound....
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose....
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...
1) SHOW WORK STEP By STEP below is Figure 7-3 Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
Could u please help me with numbers 1, 8, 9, 2, 3, 4 and also the...
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...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
please help!! switching to all online is so hard 50. When the following Fischer projection closes,...
please help!! switching to all online is so hard
50. When the following Fischer projection closes, which is the alpha Haworth form? CH2OH EO A 7 Но он se a cozycy A) a CH2OH a on B) HONE LOH HO CH₂ OH HO C2 C3°" cho CH2OH Lornoon E) Two of these are correct 51. What is the correct relationship between the 2 compounds? CH₂OH сом C=O 40 - OH HOH CH₂OH A) diastereomers B) epimers C) enantionmers and H0+...
1. Which of the following is an aldohexose? 2. Which of the following is a cetopentose? 3. Which of the following best d...
1.
Which of the following is an aldohexose?
2. Which of the following is a cetopentose?
3. Which of the following best describes the relationship
between D-glucose and D-fructose?
4. Which of the following is (are) L-alfohexose(s)?
5. Which of the following aldohexose(s) is (are)
dextrorotatory?
6. How many stereoisomers are possible for L-galactose? Draw
or look for its structure.
7. Which of the following conpounds is a pair of
enantiomers?
8. Draw the fisher projection for L-sedoheptulose and also...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocy...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocyclic amines i Cho OH HOH OH LCH, HOW N & CH₂ IN-CH HO (e) (b) 11. What is the IUPAC har is the IUPAC name of the following compound pound? OOH 9 TOH OH 9 hydroxy-1.4-dimethyl-5-oxohexanoic acid hydroxy-2-methyl-5-oxohexanoic acid (d) 2-hydro ydroxy-2,5-dimethyl-6-oxoheptanoic acid 2-hydroxy-1-methyl-4-oxopentanoic acid (e) 3-hydrox 3-hydroxy-2,5-dimethyl-5-oxohexanoic acid O 3-hydroxy-2,5-dimethy 12. Predict the product/s, the product/s, if any,...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
For each of the disaccharides or polysaccharides select from the response list the correct hydrolysis products. Responses may be used more than once or need not be used at all. a) glucose only b) glucose and galactose c) glucose and fructose d) glucose and ribose 35. Sucrose 36. Lactose 37. Cellulose 38. Starch 39. Glycogen For each of the disaccharides or polysaccharides select from the response list the correct characterization of the type of glycosidic linkages present in the compound....
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...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
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...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
please help!! switching to all online is so hard
50. When the following Fischer projection closes, which is the alpha Haworth form? CH2OH EO A 7 Но он se a cozycy A) a CH2OH a on B) HONE LOH HO CH₂ OH HO C2 C3°" cho CH2OH Lornoon E) Two of these are correct 51. What is the correct relationship between the 2 compounds? CH₂OH сом C=O 40 - OH HOH CH₂OH A) diastereomers B) epimers C) enantionmers and H0+...
1.
Which of the following is an aldohexose?
2. Which of the following is a cetopentose?
3. Which of the following best describes the relationship
between D-glucose and D-fructose?
4. Which of the following is (are) L-alfohexose(s)?
5. Which of the following aldohexose(s) is (are)
dextrorotatory?
6. How many stereoisomers are possible for L-galactose? Draw
or look for its structure.
7. Which of the following conpounds is a pair of
enantiomers?
8. Draw the fisher projection for L-sedoheptulose and also...
10. Which of the following roduct, if any, is not a heterocyclic amine? CHE HCNN Ho all of them are heterocyclic amines i Cho OH HOH OH LCH, HOW N & CH₂ IN-CH HO (e) (b) 11. What is the IUPAC har is the IUPAC name of the following compound pound? OOH 9 TOH OH 9 hydroxy-1.4-dimethyl-5-oxohexanoic acid hydroxy-2-methyl-5-oxohexanoic acid (d) 2-hydro ydroxy-2,5-dimethyl-6-oxoheptanoic acid 2-hydroxy-1-methyl-4-oxopentanoic acid (e) 3-hydrox 3-hydroxy-2,5-dimethyl-5-oxohexanoic acid O 3-hydroxy-2,5-dimethy 12. Predict the product/s, the product/s, if any,...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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