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2) (13 Pts) Write the product(s) of the following reaction and answer questions a-d. СН2ОНЫ Disaccharide...
2) (13 Pts) Write the product(s) of the following reaction and answer questions a-d. CH2OH HO HO- OH Disaccharide x H2O, HCI, 35°C -CH2OH -ОН НО. OH a. Is Disaccharide x a reducing sugar? b. Does Disaccharide x undergo mutarotation? c. Does the Disaccharide x be digests by the human's ezymes? d. Write the common name of one of the product(s)
2) (13 Pts) Write the product(s) of the following reaction and answer questions a-d. CH2046 Disaccharide x H20, HCI, 35°C HO HO OH CH2OH -OH НО. OH a. Is Disaccharide x a reducing sugar? b. Does Disaccharide x undergo mutarotation? c. Does the Disaccharide x be digests by the human's ezymes? d. Write the common name of one of the product(s)
Write the product(s) of the following reaction and answer questions a-d. CH2016 Disaccharide x H2O, HCI, 35°C HO HO OH -CH2OH ОН НО. OH a. Is Disaccharide x a reducing sugar? b. Does Disaccharide x undergo mutarotation? c. Does the Disaccharide x be digests by the human's ezymes? d. Write the common name of one of the product(s)
Answer the following questions about the reactions and
properties of the disaccharide below, which is composed of two
D-mannose units.
Answer the following questions about the reactions and properties of the disaccharide below, which is composed of two D-mannose units. Н CH2OH НО- Н но ҪH-ОН НО- Н НО НО Н В Н Н (1) What are the functional groups at C1 in unit A and C1' in unit B? (2) Is this disaccharide a reducing sugar? Explain (3) Will...
) (30 Pts) Provide the structure(s) of the expected major organic product(s). Unless mentioned otherwise, you can assume that all reagents are present in one mole. Show stereochemistry where needed and write NR if there is no reaction. о ОН E) NaOH, H2O АллОН ОН F) СН2ОНО. ОСН3 H НО H2O, HNO3, 60 °C Н. ОН CH2OH H
Write the product/s in each of the following reactions. If a racemic mixture is a product of the reaction, write structure of both enantiomers. Assign absolute configuration (R or S) of the starting compounds and final 1 compounds in a case they possess a stereogenic center. (2.5 x 10 25 points) pyridine = v a. - ONa ? Pyridines byрroduct b. S-Ci NH2 (RZ-pent-3-en-2-ol pyridine excess с. FC CF3 NaCCCH он pyridine d. Вгz. Но 1 mol NaOH cis-pent-2-ene е....
What is (are) the product(s) of the following reaction? 1. RСОН 2. НО, НО ОН ОН ОН ''ОН ОН ОН ІІ ІІ Only I and II Only | Only III Only II What is (are) the product(s) of the following reaction? 1. KMnO, 2. НО, НО ОН ОН ОН ''ОН ОН он ІІ IV || O IV What is the reagent required to accomplish the following transformation? OH OH PCC/CH2Cl2 [1] OsO4; [2] NaHSO3, H2O RCO3H, H2O/HO LiA1H4
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Determine the product of the following reaction. HCI ? ОН CI ОН CI С СЕ О ОН CI None of these products will be formed. СІ ممر ОН Predict the product of the following intramolecular Aldol reaction. NaOH, HAO A i H H o Predict the product of the following reaction. H NOH H NO ONH2 НО. 'N НО. NHOH O HOH HOONH2
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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...
Which is the major product of this reaction? CN 1. Et MgBr 2. acid workup our order on one A B C D A B С D Which compound is a D-isomer? Н. Н. T НО- -Н НО——н НО -Н Н——он Но——Н НО- H -Н он І Н. -он H- -он НО -Н НО -Н CH2OH НО- Н -ОН НО -Н СН2ОН Н. -он НОН Сньон CH OH А B с D OA B Ос D