What is true about this reaction? + A) The chlorine is the nucleophile B) The nitrogen is the leaving group C) This is an S 1 reaction because there's a carbocation D) This is an E2 reaction because of the negative charge E) This is an Sy2 reaction

This image is the final product that is produced. If a synthesis started with benzene and other organic compounds (four carbons or less) what would the synthesis look like to achieve this final product.

Draw the structure of the product of the reaction.

Name the product for the following reaction

4a. Which type of molecule is this? Label the nonpolar and polar regions of this molecule. Label the ester bonds and phosophodiester bonds. H₂C-0-C HC-0-C CH, CH,−N O CH₂ O CH3 4b. What products would you obtain if you performed an hydrolysis reaction? Draw them. O=C O=0

solve this reaction and show the product

What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? A. The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile B. The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile C. The oxygen of the carbonyl group can attack the carbon of the carbonyl group D. Only esters can undergo self-condensation reactions

Look at the atom in each molecule and classify as an electrophile or a nucleophile. How do you know if it is a electrophile or nucleophile? What makes it an electro or nucleophile? C in CH3Br  N in NH3 O in HO-

10) What primary metabolites are the building blocks of this natural product Br Br

Draw the structure of the product.