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2) (13 Pts) Write the product(s) of the following reaction and answer questions a-d. CH2046 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)
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)
2) (13 Pts) Write the product(s) of the following reaction and answer questions a-d. СН2ОНЫ Disaccharide x H2O, HCI, 35°С НО НО ОН CH2OH ОН НО. ОН
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...
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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...
(5 Marks) B. Answer the questions based on the structures given below i. ii. нонс нонс OH CH HOR OH HO CHOH CH, OH CH OH HO HOM H -OH CH, OH c. Identify the compounds ii, iii and iv as D or L. Explain how you came to this conclusion (2 marks) d. Draw the Fischer projection, enantiomer and indicate which carbons are chiral or achiral for the compound ii. (3 marks) e. Among the compounds iii and iv...
2) (40 pts) Predict the product(s) of each of the following reactions. in m radical initiator НО / HO K,Cr,07 TY OH H,804 o excess H, Pt ОН Lout Thebe + - OH NH2 A + Yo Maryl НО, OH Z HO heat ΝΗ + HCI 1) SOCI, OH 2) HNCH door de OH
13. Draw the organic product(s) of each reaction below. If no reaction will occur, then indicate that. (8 points) CN HCI, H20 + но 25 °C H2N 'Y -H20 (2 equiv.) NH D 1. NaOH, H20, heat 2. Acid work-up
1. Write structures for the lettered organic product(s) in the following reactions: (4 pts each) H, CH2OH A 1) CHCI B 2) OH OH O== + с D + E Conc. KMnO4 OH/H,0 OH PBrz F CH2CH MgBr CH3MgBr H H30 1) 03 2) Zn, H20 2Eq. HBT H3C-CEC-H NaH H3C-C=C-H K
Help sos
1. Show the expected product(s) of the following reactions. For products containin or cis/trar asymmetric carbon atoms, indicate relative stereochemistry (syn/anti relationships) and/or whether a racemic mixture is produced. (8 pts each) 1. HNO3, H2so4 NO 2. Fe, HCI OCH3 3. NaNO2 aq. HCI 4, CuCN, Δ сно но 1. Br2 H20 2. Fe SO)S b. HO- -H OH s CH2OH 1. SOCI2 2. NH3 H3C 3. Br2 NaOH, H2O 1. KOH 2. PhCH2CH Br 3. NH2NH2 d....