Choose the answers that show structures that will not form the product shown: CH OH IV Cro O 1, II, IV II, IV

2. Using the following structures (all C7H120) as a guide, choose the ONE best answer for each of the following: OH OH C E F

During multistep syntheses, reduction reactions are often performed. Functional groups react differently with these reagents. With this in mind, draw the structure of the product of this reaction: NH2 NH2 LIAIH4 OH HO2C CO2H ČO2H For your convenience, the starting material has been drawn for you in the sketchpad. P aste opy C NH2 NH2 OH HO, HO

Predict the organic product(s) of the following reactions.

A chemist synthesized compound X as a racemic mixture. When the ketone group in X was enzymatically reduced to the corresponding alcohol, a 100% yield was obtained of the product shown below. Choose the statement that best describes this result. ОН enzyme C;H1 `OCH,CH; pH 4.0 C3H1 `OCH,CH3 ОН ÕH X (racemic) (100% yield) One enantiomer of compound X reacts quickly with the enzyme. The other enantiomer of compound X is unreactive, but rapidly equilibrates with the reactive enantiomer under the reaction conditions. Since compound X was racemic, it makes sense that only a single product was obtained. O The product is a meso compound, so either enantiomer of compound X gives the same product. One enantiomer of compound X reacts quickly with the enzyme, while the other enantiomer of compound X remains unchanged.

Predict the major products of this organic reaction. : ☐ + Х 1.03 2. Zn, H₂O

2. Starting from benzene, how can you synthesize the following molecules? NH2 CO₂H OH CI OH CO₂H CI CO₂H £ 5 & 2 4 4 or Br Br NO2 SO3H

Predict the product...

Please answer both, thank you so much!

Please help with the following... Draw the bond line structures for the reactants and the products obtained in the following reactions: 1. m-chlorocumene +NaNiPr2, HNiPr2 2. 4-tertbutyl-3-methyl anisole + HNO3, H2SO4 3. o-isopropyl acetophenone + PhCH2COCl, AlCl3