
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:Draw 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 Draw
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- Give exarrow_forwardCurved 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. I I HH :CI. co THE I Select to Edit Arrowsarrow_forwardSee image belowarrow_forward
- Don't use hand raiting please larrow_forward2. For the acid/base reaction below: a. Draw electron-pushing arrows to show how the reactants are converted to the products. b. Circle the side of the equilibrium that is favored. mot c. Draw a reaction coordinate diagram for the acid/base reaction. E reaction coordinatearrow_forwardd) a) O OEt -Ome 1. NaBHY, Mеoн 2- HCl (da) 1. LIATHY, MeOH на (аа) 2. 1. LAIHY, THE HCl (aq) INABHY, MCGH → 2. HCI (aa) draw product draw product draw product draw productarrow_forward
- K Draw the initial organic product of the Bronsted acid- base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. H3O+ Drawing Question 5 Atoms,arrow_forwardIn the following acid-base reactions, 1. draw Lewis structures of the reactants and the products. 2. determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). 3. use the curved-arrow formalism to show the movement of electron pairs in these reactions, as well as the imaginary movement in the resonance hybrids of the products. 4. indicate which reactions are best termed Brønsted-Lowry acid-base reactions. (c) -BH₁₂ BH3 + CH3-O-CH3 → CH3-O-CH3 (d) 유 0- CH3-C H + -OH CH₁₂-C-H OHarrow_forwardPlease provide explanations and workarrow_forward
- 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) Harrow_forwardWhat is the outcome of the reaction sequence shown in the box? 1. Base 2. Allylbromide ? H3CO 3. НСІ, Н,О, НЕAТ A) B) Но C) D) A, B.arrow_forwardHighlight in red each acidic location on the organic molecule at left. Highlight in blue each basic location on the organic molecule at right. Note for advanced students: we mean acidic or basic in the Brønsted-Lowry sense only. NH₂ NH₂ × Garrow_forward
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