Click the "draw structure" button to launch the drawing utility. Draw the intermediate in this stepwise reaction sequence that uses proton transfer reactions to convert the starting material to the product. Since this intermediate is resonance stabilized, draw any one of its resonance structures for credit. Do not include lone pair electrons in your answer. (Hint: As a first step, use OH to remove a proton from the CH₂ group between the C=O and C=C.) 3- 3 + -OH + OH → H₂O (solvent) draw structure ... (organic intermediate) -&

Draw the major product of this acid-base reaction. Include all lone pairs. Ignore inorganic byproducts. :0: H NaNH2 Q

3) Use the reaction shown below and the associated reaction energy diagram to answer the following questions. E A Но- + Br HO. Br- reaction coordinate a) In the space above, use curved arrows to show the mechanism of the reaction. b) Classify the reaction as either addition, elimination or substitution. c) In this reaction is hydroxide (HO-) acting as a nucleophile or as a base? c) Based on the reaction energy diagram, is the reaction endergonic or exergonic? d) Based on the reaction energy diagram, and assuming the reaction is reversible, would the equilibrium lie to the left or to the right? e) Which position on the reaction energy diagram (A, B or C) corresponds to the transition state?

Draw all intermediates and show all electron-pushing.

Choose the one has the highest priority, and the one has the lowest. (Please show why) -CHO -COOH -COCH3 -CONH2

Draw the reactant of the following reaction. ? OH heat

10:54 ← Question 21 of 32 Draw the major product of this reaction. Ignore inorganic byproducts. Submit Assume that the water side product is continuously removed to drive the reaction toward products. (CH3)2NH, TSOH Select to Draw | I I

Hello! Can someone please help me with this question?

Add curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to represent the movement of a pair of electrons. Draw curved arrows. Select Draw Rings More Erase | : 0 H-O: H OH

Complete the electron‑pushing mechanism for the given decarboxylation reaction. Add bonds, nonbonding electron pairs (lone pairs), and curved arrows where indicated.