An unknown pentose Z reacts with NaBH4 to give an optically inactive compound. The pentose Z gives the same osazone as arabinose. What carbohydrate is Z?
Ribose |
Xylose |
Glucose |
Fructose |
Lyxose |
An unknown pentose Z reacts with NaBH4 to give an optically inactive compound. The pentose Z give...
What is the identify of compound A and B? D-allose L-allose D-altrose L-altrose D-arabinose L-arabinose D-erythrose L-erythrose D-erythrulose L-erythrulose D-fructose L-fructose D-galactose L-galactose D-glucose L-glucose D-glyceraldehyde L-glyceraldehyde D-gulose L-gulose D-idose L-idose D‐lyxose L‐lyxose D-mannose L-mannose D‐psicose L‐psicose D-ribose L-ribose D-ribulose L-ribulose D-sorbose L-sorbose D-tagatose L-tagatose D-talose L-talose D-threose L-threose D‐xylose L‐xylose D-xylulose L-xylulose None of the above What is the identify of compound A? CH2OH HO OH OH OH Compound A
Please answer in full An unknown pentose (C_5H_10O_5) A is treated with conc. HNO_3 giving optically inactive diacid B. Kiliani-Fischer chain elongation of A results in the formation of two epimeric hexose sugars, C and D, whose diacids (from HNO_3 oxidation) are both optically active (E and F, respectively). When subjected to the Fisher sequence (C1 - C6 interchange), hexose D affords L-glucose. Treatment of pentose A with aqueous bromine gives G, which undergoes decarboxylation in the presence of iron...
1) An unknown compound "X' with formula C.HCl reacts with a bulky a base to give only one product Y' with the formula CHio. Y reacts with hot KMnO4 to give C.H..0.. Draw the structural formulas for X, Y, and Z (12 points)
an unknown compound b and formula c6h11cl reacts with a bulky base and gives product y and formula c6h10. y then reacts with kmno4 and gives C6H10O4. what are the b, y and last product?
MAKE IT LEGIBLE!!!! ASAP PLS!!! An unknown compound 'X' with formula C6H11Cl reacts with a bulky a base to give only one product ‘Y' with the formula C6H10. 'Y' reacts with hot KMnO4 to give C6H1004. Draw the structural formulas for X, Y, and Z.
pppppplllleeeaaassseee help 1. a. Compound 1 reacts with A under acid conditions to form an imine. What could Z be in this reaction? b. Compound 2 reacts with A (same A as previous reaction) under acid conditions to form an amide. What is Z in this reaction? Draw the structure of A Use curved arrows to show how Compound 2 forms the amide. c. Both reactions involve a leaving group. What is the leaving group in each reaction? O A...
Chern 204-PSI, 6 . Friedel Crafts Acylation of an Unknown Benzene Compound (One weck lab The Intent of this Lab To acetylate an unknown benzene compound via a Friedel-Crafts acylation and use spectroscopic techniques to determine the acetophenone derivative's identity Introduction The Friedel-Crafts reaction dates back to before 1900 and it is still widely used today. The active electrophilic agent (an acylium ion) is classically prepared and reacts very quickly. Another appealing feature of this reaction is that the acylated...
thats all the information that he gave us to solve the question. Thank you for trying anyways X C E Question 23 1 pts The free-energy changes for the transfer of individual amino acid residues from a hydrophobic to an aqueous environment are given as follows: Amino acid AG of transfer (kJ/mol Proline -0.8 -12.6 Histidine 6.7 Alanine Methionine 14.3 Based on this information, which of these amino acid pairs is MOST likely to be represented in membrane-spanning alpha helices?...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...