A correct order of reactivity of acid derivatives towards nucleophilic attack is ________.   Question 4 options:   esters > amides > anhydrides   anhydrides > amides > esters   acid chlorides> anhydrides > amides    esters > acid anhydrides > amides   anhydrides > esters > acid chlorides

Please help with this question question 9

please help?

which is the product formed when thus compound is hydrolized in aqueous acid   Please don't provide handwriting solution

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: 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. бль EtO OEt Edit Drawing

Explain the differences in pKa (vs. benzoic acid) of these substituted benzoic acids based on fundamental chemical principles (not just what pKa means).

Could I please have help with number 5: Show the full structure of the salt that forms when triethylamine reacts with hydrochloric acid

5. Circle the carbon atom that contains the most acidic C-H bond in this molecule e 6. The tertiary amine and aldehyde below will react to form a. An imine b. An enamine c. A nitrile d. None of the above 7. The secondary amine and aldehyde below will react to form HN, a. An imine b. An enamine c. A nitrile d. None of the above

If propionic anhydride is added to a/an [Select] [Select] thiol amine amide alcohol it will form a thioester.

Draw the reactants and products of the azo dye synthesis. Cl. NH₂ Primary Amine #21 #16 NaNO₂ Azo Dye Activated Aromatic -OH