which reagent can convert the glucose ring into a linear chain?
A) HCL (aq)
B) H2CrO4
C) NaOH (aq)
D) two of the above
E) all of the above
which reagent can convert the glucose ring into a linear chain? A) HCL (aq) B) H2CrO4...
Glucose-6- chosohate S! After the glucose ring opens, an isomerization occurs to convert the aldohexose (1) into a ketohexose (3) via the enediol intermediate shown (2). Show "arrow pushes on structure (1) which will which convert it to structure (2),a show "arrow pushes" on structure (2) which will convert it to structure (3). (Use "B:" to deprotonate and "H-B" to protonate) о-н H-I Ho- 4 t-1 t o-H CI) 9a. The key step in the catabolism of glucose is a...
8. After the glucose ring opens, an isomerization occurs to convert the al enediol intermediate shown (2). Show "arrow pushes on structure (1) which will which convert it to dohexose (1) into a ketohexose (3) via the common structure (2), and pushes" on structure (2) which will convert it to structure (3). (Use "B:" to deprotonate and "H-B" to protonate). o-H C-o-H it CI) 2. 9a. The key step in the catabolism of glucose is a retro-aldol condensation of the...
A solution contains either Ag+(aq) or Fe3+(aq). Which chemical reagent would NOT allow you distinguish which cation is in the unknown? A. C2O42- B. HCl C. KSCN D. HNO3 E. all of these reagents would work to distinguish the ions
5. Which combination will produce a precipitate? a) NH4OH(aq) and HCl(aq) b) AgNO3(aq) and CaCl2(aq) c) NaOH(aq) and HCl(aq) d) NaCl(aq) and H2SO4(aq)
D-glucose is shown below in its straight-chain and ring forms. A) Put an asterisk next to each chiral carbon in the straight-chain form of D-glucose. B) Label the given ring forms as the alpha or beta anomer of D-glucose. Draw the other anomer. Which one is more stable, the alpha or beta anomer? Explain your logic. H Он он но H Но Но Н он H он он н но но
Which reagent is required in the box for Reaction 1? A) CrO3, HCl, Pyridine B) LDA C) HBr D) NaOH E) TsCl w/ pyridine F) PBr3 G) LiAlH4 Consider the structures of Intermediate Product Y and the final product. What would be the best reagent to place in the box for Reaction 2? A) H2O B) NaOH C) Mg D) (CH3)3COK E) NaBH4 F) HCl G) CH3Br E) CrO3, H2SO4, H2O 11 Reaction 1 Intermediate Product Y Reaction 2 HO
Which of the following reagent(s) eves the reaction below (A) CH_2Cl (B) Cl_2/Fe (C) Cl_2/AlCl_3 (D) Cl_2/FeCl_3 (E) Cl_2/HCL Which of the following reagent(s) gives the reaction below (A) NaOH (B) KMnO_4/H_2O (C) Sn/HCL, then NaOH (D) CO_2/H^+ (E) O_2/HCl Which of the following reagent(s) gives the following transformation (A) CH_3COCI/AICI_3, then NaOH (B) CH_3COCl/AlCl_3, (C) CH__3CH_2Cl/AlCl_3, then NaBH_4 (D) CH_3CH_2Cl/AICI_2 then PCC (E) CH_3COCI/AICI_3 then NBS Which of the following reagents (a, b) gives the reactions below (A) a...
A 100.0 mL sample of 0.400 mol L-1 HCl(aq) is added to 150.0 mL of 0.300 mol LNH3(aq) (which can be thought of as a solution of NH4OH) in a coffee cup calorimeter and the temperature of the resulting solution rises from 23.92°C to 26.07°C. HCl(aq) + NH,OH(aq) → NH.Cl(aq) + H2O(1) (a) Determine the limiting reagent. (b) Calculate the enthalpy change, A.H.
This solid compound can be hydrolyzed in aq NaOH ( heating under reflux ) Above compound was reacted with NaOH and then mixture was cooled. After cooling HCl was added and precipitates were seen. a) draw the structure of precipitate and species containg benzene ring before the addition of HCl b) show the mechanism of how the species containing benzene ring before the addition of HCl was formed 0 ОН
1. Draw glucose B-D-glucose in a chair form, and circle the anomeric carbon. Why is the anomeric carbon significant? 2. Why is cyclization of sugars important? What does the concept of mutarotation indicate to us about dual roles of monosaccharides? Two part question: 3. Why are monosaccharides most commonly found in pyran and furan ring forms, rather than: A) other ring motifs -(think along the lines of: why NOT 3,4, or 7 membered rings)? B) in their linear form? 4....