An unknown carbohydrate could be reduced by a series of steps to a compound with five carbons. It does give a positive Benedicts test and it has two chiral carbons. What is the structure consistent with these facts?
Alkane Reactions - An unknown compound with a molecular formula of C8H18 reacts with chlorine in the presence of light and heat. From the reaction, only one compound with the formula C8H17Cl can be isolated. What is the ...
Identifying 4 unknown compounds - Compound A (C7H14) decolorized a Br2-CH2Cl2 solution. It reacted with BH3*THF reagent, followed by alkaline peoxide solution, to produce Compound B. Compound B on treatment with chromic-acid sulfuric ...
Identifying another 3 unknown compounds - An unknown compound (A) was soluble in ether but only slightly soluble in water. It burned with a clear blue flame and combustion analysis showed it to have a molecular formula of C5H10O. It gave a po ...
Identifying unknown substances - Compound A (C7H14O) burned with a yellow, nonsooty flame and did not decolorize a bromine-methylene chloride solution. It did give a positive 2,4-dinitrophenylhydrazine test, but a negative Tollens te ...
H NMR and C NMR - Each word document contains one problem. I need the structures that go along with each spectrum.
See attached file for full problem description.