Draw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. H₂O* Drawing 'H
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- In the following acid - base reactions, a) Draw Lewis structures of the reactants and the products. b) Determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). c) Use the curved - arrow formalism to show the movement of electron pairs in these reactions and the imaginary movement in the resonance hybrids of the products. d) Indicate which reactions are best termed Brønsted-Lowry acid - base reactions i. CH3CHO + HCI-- > CH3CH2O + + Cl- ii. CH3CHO + OH- - - > CH3CO-(OH) HDraw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. C:O HCI Select to DrawDraw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. HCI C
- Use curved arrows to show the most likely acid-base reaction between phenol and NaOH. a. Use pKa data to mark each curved arrow with a positive or negative energy change in pKa ,units. b. Calculate H for this reaction, and sketch an energy diagram showing H as an arrow onyour diagram.4. Draw the structure and name the first ten (10) members of Acid Halides using bromine as the halide.Organic Chemistry II: How do we know which direct the reaction? Why Methoxy Functional Group direct the reaction instead of fluorine? Is it something to do with electronegativity ? Or is it something to do with withdrawing group?? How do we know if a gourp is more withdrawing ??????
- help; please DRAW IT; don't answer in text. thanks the reactions are all covered in Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise. Chapter 15-173) 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?What would be the final product(s) of each of the conditions (base and temperature) for the reaction attached. r.t. = room temperature.
- What reaction will occur when benzoic acid is mixed with sodium bicarbonate? (Hint: benzoic acid is an acid and sodium bicarbonate is a base...) What three products will be generated by this reaction? (You may have to look this one up...) HO. Na HO.Curved arrows are used to illustrate the flow of electrons. In this reaction, a pi bond acts as a Bronsted base. Using the provided starting structures, draw the curved electron-pushing arrows for the acid-base reaction. Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of the reaction. Include all lone pairs in the structures. Ignore inorganic byproducts and counterions. H. | H H :CIⒸ Select to Add ArrowsDraw the organic product structure formed by the reaction sequence. Draw the product. Select Draw Rings More Erase H 1. B2H6, diglyme 2. NaOH, H2O, H2O2