• HO- CHO -OH pyranose form(s) -OH -OH CH₂OH D-glucose Use the wedge/hash bond tools to indicate stereochemistry where it exists. If two diastereomers are formed, draw both. If no reaction occurs, draw the organic starting material. Draw carboxylic acids in neutral (unionized) form. Use "flat" representations of rings, not chairs, in your drawing. Do not draw your answer as a Haworth projection. {n [ ?

Organic Chemistry

Question 2 Which statement is consistent with the Hammond postulate? O the transition state of an endothermic reaction step structurally resembles the reactant. O it is used to assign the E/Z stereochemistry of alkenes. the less stable carbocation intermediate is formed in electrophilic additions to alkenes. O in additions of HX to alkenes, the H adds to the less substituted alkene carbon and the X adds to the more substituted alkene carbon. O the transition state of an exothermic reaction step structurally resembles the reactant. A Moving to another question will save this response. 80 F3 54 $ 4 000 000 F4 % 5 F5 6 MacBook Air F6 & 7 ao F7 8 DII F8 ( 9 F9

What is the correct answer and why?

Is C-O ester of 3-chloro-4’-methoxychalcone conjugated (talking about the H3CO attatched to the benzene ring)? Can you explain your answer?

Give a brief answer to explain why acetic acid has a much higher BP (118 C) than 1- propanol (BP = 97 C) even though they both have the same size (molecular weight = 60) and they both form Hydrogen bonds.

Draw the structure of the major organic product obtained by hydroboration-oxidation of trans-3-methyl-3-hexene. H Click and drag to start drawing a structure. : ☐ G P

O H+ (cyclic ester) HOCH2CH2CH2-C-OH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. If there is no reaction, draw the organic reactants.