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six questions plz help i leave rating
The missing product from the following reaction is OH...
I need some help to answer these following questions. Thanks. 41. Which molecule(s) is/are aromatic? I1...
I need some help to answer these following questions.
Thanks.
41. Which molecule(s) is/are aromatic? I1 IV (A) I only (C) I, III, and IV (B) I and IV (D) I, II, III, and IV OH OH 42. Which Fischer projection represents this structure? HO OH OH H CHO CHO (A) H-OH (B) HOH HOH CH2OH CH2OH CHO HOH CHO но -н CH2OH CH2OH 43. Which is a product of this ozonolysis reaction? 1.03 2. (CH3)2S H O I BHs/THF...
i need help plz with #5 with explanation thanks :) 126 Give the major product(s) for the reaction. 5. CH2OH Krtone 1...
i need help plz with #5 with explanation thanks :)
126 Give the major product(s) for the reaction. 5. CH2OH Krtone 1. NaBH но CH:OH CH2OH CH20H CH20H CH2OH 2OH OH HO Ho OH OH H он OH CH2OHV CH20H CH2OH II OH CH20H Ryl II and IV D) IV and V A) 1 and II II and III
126 Give the major product(s) for the reaction. 5. CH2OH Krtone 1. NaBH но CH:OH CH2OH CH20H CH20H CH2OH 2OH OH...
plz help 9. What would be the major product of the following reaction? H2O+ CHECCHCH2CH3 +...
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9. What would be the major product of the following reaction? H2O+ CHECCHCH2CH3 + Brz ? CH3 Br OH i OH concen CBH CCHCHCH3 C6H5CcBrCH2CH3 CeHCCHCHCH3 Corsa CH3 CH3 CH3 C. B. A. CeHCBr2CHCH2CH3 məcsidcmen.com m-BrCH CCHCH2CH3 D. CH3 E. CH3 10. What would be the product, C, of the following reaction sequence? OH H307, heat НА COH CH + CH3CH2CH 25 °C (-H,0) i H2, Ni high pressure corporal CHECCHCH2OH CH3 CHCH2CHCH2OH B. CHE CeHCH,CHCH сн. A....
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates...
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates 11) Mochides will C Moncuccharides tuve i detyder skete D) Mononcerides centove or more alcohol group 26. Which of the following tyres of hohydrates can be hydrolyzed to give smaller molecules? 1. Monosaccharides 1 Disaccharides TIT. Oligosaccharides IV. Polysaccharides A) I only B) II and IV only C) III only D) I and II only E) II. HII and IV C) 4 27. The...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent a monosaccharide, a disaccharide, a trisaccharide or something else? B Are any chiral carbons present? If so, circle each one. C Does this represent an aldose or a ketose? Explain your response and draw a box around the relevant functional group. D Give the molecular formula for this compound. E Is this compound classified as an L-isomer or a D- isomer? your response. Explain...
35. Enzymatic processing to break down glycogen into glucose occurs at: a. a reducing end. b....
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...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D)...
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....
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C B...
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
I need some help to answer these following questions.
Thanks.
41. Which molecule(s) is/are aromatic? I1 IV (A) I only (C) I, III, and IV (B) I and IV (D) I, II, III, and IV OH OH 42. Which Fischer projection represents this structure? HO OH OH H CHO CHO (A) H-OH (B) HOH HOH CH2OH CH2OH CHO HOH CHO но -н CH2OH CH2OH 43. Which is a product of this ozonolysis reaction? 1.03 2. (CH3)2S H O I BHs/THF...
i need help plz with #5 with explanation thanks :)
126 Give the major product(s) for the reaction. 5. CH2OH Krtone 1. NaBH но CH:OH CH2OH CH20H CH20H CH2OH 2OH OH HO Ho OH OH H он OH CH2OHV CH20H CH2OH II OH CH20H Ryl II and IV D) IV and V A) 1 and II II and III
126 Give the major product(s) for the reaction. 5. CH2OH Krtone 1. NaBH но CH:OH CH2OH CH20H CH20H CH2OH 2OH OH...
plz help
9. What would be the major product of the following reaction? H2O+ CHECCHCH2CH3 + Brz ? CH3 Br OH i OH concen CBH CCHCHCH3 C6H5CcBrCH2CH3 CeHCCHCHCH3 Corsa CH3 CH3 CH3 C. B. A. CeHCBr2CHCH2CH3 məcsidcmen.com m-BrCH CCHCH2CH3 D. CH3 E. CH3 10. What would be the product, C, of the following reaction sequence? OH H307, heat НА COH CH + CH3CH2CH 25 °C (-H,0) i H2, Ni high pressure corporal CHECCHCH2OH CH3 CHCH2CHCH2OH B. CHE CeHCH,CHCH сн. A....
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates 11) Mochides will C Moncuccharides tuve i detyder skete D) Mononcerides centove or more alcohol group 26. Which of the following tyres of hohydrates can be hydrolyzed to give smaller molecules? 1. Monosaccharides 1 Disaccharides TIT. Oligosaccharides IV. Polysaccharides A) I only B) II and IV only C) III only D) I and II only E) II. HII and IV C) 4 27. The...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent a monosaccharide, a disaccharide, a trisaccharide or something else? B Are any chiral carbons present? If so, circle each one. C Does this represent an aldose or a ketose? Explain your response and draw a box around the relevant functional group. D Give the molecular formula for this compound. E Is this compound classified as an L-isomer or a D- isomer? your response. Explain...
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...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
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....
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
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