In the following molecules, the carbon with the double bond to oxygen is called the carbonyl carbon. Which molecule has the more electrophilic carbonyl carbon? Explain your reasoning.

Rank the acidity of each of these compounds from least to most acidic. The explicitly drawn Hydrogens should be compared. What would be a small explanation as to why they are ranked in that order?

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

a) b) C) Show the steps necessary, in order, to make each of the following compounds. Start with benzene, and use only reactions we studied this semester. O 10₂ NO₂ -ECH₂CH3 o Br

Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compounds below with base.

Subject :- Chemistry

eq eq M M M ereg 2req 2req 2req X 2req J F3 $ 4 R C V [Review Topics] [References] Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. 4x Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. ✓✓99.81 O 0- F4 . % 5 T G B F5 *** ^ 6 Cengage Learning Cengage Technical Support Y ChemDoodle H N F6 & N& 7 U O J F7 + [ ] در M 8 PrtScn K F8 9 Home O 83°F Sunny F9 L ) 0 End F10 P Previous C PgUp F11 9 ? Next Save and Exit 9:38 AM 7/18/2022 PgDn F12 0 Ins D Back

Q2Show why the OH functional group, of phenol below, is ortho directing using curly arrows to show the formation of each of the four resonance structures A, B, C and D. Draw all the resonance structures A through D and explain why one resonance structure is more favourable than the other three in directing the electrophile (E*) ortho to the OH functional group.