The conjugate base of diethyl malonate can serve as a nucleophile to attack a wide range of electrophiles. Identify the product that is formed when the conjugate base of diethyl malonate reacts with the following electrophile followed by acid workup when relevant: CN Modify the provided structures of diethyl malonate and the given electrophile to draw the product formed. Note: the eraser tool can be used to erase bonds, and atoms can be moved by selecting them with the selector tool and then dragging the selected atom(s) to a new position. If you make a mistake, you can use Ctrl-Z or the Undo tool. EtO OEt H3C CN

The analgesic Tylenol is often taken by people who are allergic to aspirin. Tylenol contains acetaminophen (structure shown) as the active ingredient.   Is the structure of acetaminophen similar to the structure of aspirin? In what way? Would acetaminophen give a positive phenol test? What products would be obtained if acetaminophen were hydrolyzed in acidic aqueous solution?

Please help me with both these questions, i want to study today but I dont get this, please provide deep description while also making the answer clear

1. Write the general mechanism for a Nucleophilic Substitution Reaction.

Draw the structures of all possible products formed from the following reaction. Specify the type of substitution or elimination pathway. Demonstrate the sterrochemical outcomes of the reaction by drawing your products in wedge dash form when necessary.

Draw the line angle diagram of two other functional groups that act as electrophiles in the presence of a nucleophile (or basic conditions). Write the names of the functional groups under each structure.

Please don't provide handwriting solution

Please give the explanation of the concept and please provide detailed solution

draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions.

a) Put these three common types of carbonyl compound in order of decreasing reactivity         ester          amide          acid chloride           b) For the least reactive, show the interconversion to its other resonance form:         How does this electron delocalisation make it stable?         c) For the most reactive, draw the mechanism of its undergoing hydrolysis (reaction with H2O): Why makes this type of carbonyl so reactive to nucleophiles?