Draw a major resonance contributor of this enolate anion. Include all lone pairs in your structure. :0: O:☀ Drawing

Draw a major resonance contributor of this enolate anion. Include all lone pairs in your structure. O CH2 O: Atoms, Bo and Ring Draw or tap a

Draw a major resonance contributor of this enolate anion. Include all lone pairs in your structure. H H 0:01 Drawing Q

Draw the organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. •H :F: :O: :O: H Na Ⓒ 0:0- H

What would be found in an HNMR of this compound? N- O :O

20:33 1 : ●●● all the proper notations for depicting resonance. 4. Provide the full mechanism (curved arrows and intermediates) that leads to the product in the scheme below. Draw the structure of the product to help you see how the starting materials will combine. Use that as a clue to figure out how to draw the mechanism arrows. ccare in your scheme. Be sure to use NaOEt 00 i 5. Provide the major organic product of the reaction shown. Determine if these conditions are best for SN2, SN1, E2, or E1. Be sure to indicate stereochemistry by using the proper wedges/dashes in the product. acetone phenyl butanoate Send a chat O

Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. HH 1 eq. base H H H o

Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. •N₂ H H 1 eq. base H H H

How would you explain the o-p directing formation of phenol, while nitro benzene is m-directional? Explain by showing the resonance structures.

Rank the nitrogen-containing aromatic molecules in order of increasing basicity. Least basic :ZII Br CH3