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need help with 7 & 8 please
also a part D
7. How does the structure...
Choose three amino acids, no more than one of each of the following types: a. polar...
Choose three amino acids, no more than one of each of the following types: a. polar side group b. non-polar side group c. acidic side group d. basic side group Draw an unambiguous structure for each of the amino acids you chose, in the full propionate form (at pH=0). That is, all oxygen/sulfur sites should be neutral, and appropriate amino sites should have a+1 charge. For full credit, show all stereochemistry properly. a. b. c. CIRCLE the side groups for...
1. What amino acids do the following abbreviations stand for? Draw the structure of each. a)...
1. What amino acids do the following abbreviations stand for? Draw the structure of each. a) lle b) Thr c) Gin 2. Name and draw the structures of the amino acids that fit these descriptions: a) Contains an isopropyl group b) Contains a secondary alcohol group 3. Which of the following objects is chiral? a) A pair of scissors b) A comb c) A drinking glass 4. What does the term achiral mean? Give two examples involving organic structures.. 5....
please answer 8. Quaternary structure: The image below is of a polypeptide in quaternary (4°) structure...
please answer
8. Quaternary structure: The image below is of a polypeptide in quaternary (4°) structure level of protein folding. The image to the left is of hemoglobin. It is composed of four separate polypeptide chains indicated by the color differences. The image on the right indicates the backbone items as a ribbon (or line), while the side chains are chemically drawn. a. Name the specific bond/interaction indicated by the: i. Letter A ii. Letter B iii. Letter C iv....
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, n...
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, non- polar, acidic, or basic: 6 (4 pts) The amino acid threonine (thr) has two chiral carbons. Draw a Fischer projection of the 2S,3S configuration of threonine. キ 7.(11 pts) Draw the tripeptide lys-asp-ser at physiological pH 8. (8 pts) The pK, values for aspartic acid are 2.10, 9.82...
Tor F 1. With the exception of steroids, all lipids contain at least one fatty acid. 2. Some lipids contain monosaccharides as part of their structure. 3. Some lipids contain an amino acid as part of...
Tor F 1. With the exception of steroids, all lipids contain at least one fatty acid. 2. Some lipids contain monosaccharides as part of their structure. 3. Some lipids contain an amino acid as part of their structure. 4. Glycerophospholipids contain a phosphate portion in their structure. 5. All lipids have a molecule of glycerin as their backbone. 6. Polyunsaturated fatty acids have more than one C-C double bond in their "backbone." 7. Fatty acids are soluble in water. 8....
7. Draw a Fisher structure for glucose and label the chiral carbons. 8. How does an...
7. Draw a Fisher structure for glucose and label the chiral carbons. 8. How does an oligosaccharide differ from a polysaccharide? 9. In the test using Fehling's solution-What element is responsible for the color change? What is the element or compound responsible for each coter listing the color of each?
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
help please this is all the information i have, im not sure how this is incomplete...
help please
this is all the information i have, im not sure how this is
incomplete
8. Finish the LEWIS Structures for each compounds in the following reaction: H,0, +CH,OH + H.CO2H,0 How many polar molecules among the four compounds? Explain. 9. (a) Draw the Lewis structure(s) of nitrite ion. (b) Figure out the electron cloud geometry, the molecular geometry, and bond angle around the central atom. (c) Does the ion contain polar bond(s)? Is it a polar ion? Sketch...
3. (4 pts) Complete the Fischer projection drawn below by adding the four substituents to the chiral carbon of (s)...
3. (4 pts) Complete the Fischer projection drawn below by adding the four substituents to the chiral carbon of (s)-2-methyl-3-bromo-hexane. 4. (4 pts) Draw a wedge and dash structure representing (1R 2R,3S)-1,2- dichloro3-ethylcyclohexane. 5. (4pts) 2-bromobutane is shown below. Is this (R)-2-bromobutane or (S)-2 bromobutane? 6. (6 pts) For each chiral carbon in ascorbic acid (vitamin C), shown below, assign Ror S to each stereocenter. How many stereoisomers of ascorbic acid are possible? OH HO ОН 7. (9 pts) (Are...
Choose three amino acids, no more than one of each of the following types: a. polar side group b. non-polar side group c. acidic side group d. basic side group Draw an unambiguous structure for each of the amino acids you chose, in the full propionate form (at pH=0). That is, all oxygen/sulfur sites should be neutral, and appropriate amino sites should have a+1 charge. For full credit, show all stereochemistry properly. a. b. c. CIRCLE the side groups for...
1. What amino acids do the following abbreviations stand for? Draw the structure of each. a) lle b) Thr c) Gin 2. Name and draw the structures of the amino acids that fit these descriptions: a) Contains an isopropyl group b) Contains a secondary alcohol group 3. Which of the following objects is chiral? a) A pair of scissors b) A comb c) A drinking glass 4. What does the term achiral mean? Give two examples involving organic structures.. 5....
please answer
8. Quaternary structure: The image below is of a polypeptide in quaternary (4°) structure level of protein folding. The image to the left is of hemoglobin. It is composed of four separate polypeptide chains indicated by the color differences. The image on the right indicates the backbone items as a ribbon (or line), while the side chains are chemically drawn. a. Name the specific bond/interaction indicated by the: i. Letter A ii. Letter B iii. Letter C iv....
5. D-sorbital is found in 'sugar-free' chewing gum. It is formed by reducing D-glucose with NaBH Draw the structure of D-sorbital. s. (4 pts) Classify the following amino acid as polar, non- polar, acidic, or basic: 6 (4 pts) The amino acid threonine (thr) has two chiral carbons. Draw a Fischer projection of the 2S,3S configuration of threonine. キ 7.(11 pts) Draw the tripeptide lys-asp-ser at physiological pH 8. (8 pts) The pK, values for aspartic acid are 2.10, 9.82...
Tor F 1. With the exception of steroids, all lipids contain at least one fatty acid. 2. Some lipids contain monosaccharides as part of their structure. 3. Some lipids contain an amino acid as part of their structure. 4. Glycerophospholipids contain a phosphate portion in their structure. 5. All lipids have a molecule of glycerin as their backbone. 6. Polyunsaturated fatty acids have more than one C-C double bond in their "backbone." 7. Fatty acids are soluble in water. 8....
7. Draw a Fisher structure for glucose and label the chiral carbons. 8. How does an oligosaccharide differ from a polysaccharide? 9. In the test using Fehling's solution-What element is responsible for the color change? What is the element or compound responsible for each coter listing the color of each?
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
help please
this is all the information i have, im not sure how this is
incomplete
8. Finish the LEWIS Structures for each compounds in the following reaction: H,0, +CH,OH + H.CO2H,0 How many polar molecules among the four compounds? Explain. 9. (a) Draw the Lewis structure(s) of nitrite ion. (b) Figure out the electron cloud geometry, the molecular geometry, and bond angle around the central atom. (c) Does the ion contain polar bond(s)? Is it a polar ion? Sketch...
3. (4 pts) Complete the Fischer projection drawn below by adding the four substituents to the chiral carbon of (s)-2-methyl-3-bromo-hexane. 4. (4 pts) Draw a wedge and dash structure representing (1R 2R,3S)-1,2- dichloro3-ethylcyclohexane. 5. (4pts) 2-bromobutane is shown below. Is this (R)-2-bromobutane or (S)-2 bromobutane? 6. (6 pts) For each chiral carbon in ascorbic acid (vitamin C), shown below, assign Ror S to each stereocenter. How many stereoisomers of ascorbic acid are possible? OH HO ОН 7. (9 pts) (Are...
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