Complete the reaction by adding curved arrows on the left, and product structures on the right. Be sure to add lone pairs and charges and include the conjugate acid and conjugate base. H H + Add/Remove step Click and drag to start drawing a structure.
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![Complete the reaction by adding curved arrows on the left, and product structures on the right. Be sure to add lone pairs and charges and include the
conjugate acid and conjugate base.
H
H
+
Add/Remove step
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drawing a structure.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5cdcc391-5c4e-4c7f-a42a-1709b5f6cf09%2F84fcceb0-64ef-49a7-8a35-15eed70e2253%2Fd0b6u8q_processed.jpeg&w=3840&q=75)
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- For each molecule below, draw the conjugate acid or conjugate base or both if the molecule hasboth a conjugate acid and a conjugate base (e.g., water).2. Use curved arrows to show electron movement in the reactant side and draw the product/s of the Lewis acid-base (nucleophile-electrophile) reaction. Label the nucleophile and the electrophile. Draw in all lone pairs and charges where appropriate. I3. Use curved arrows to show electron movement in the reactant side and draw the product/s of the Lewis acid-base (nucleophile-electrophile) reaction. Label the nucleophile and the electrophile. Draw in all lone pairs and charges where appropriate. -co 요
- Electronegativity is favorable for nucleophilicity but not for basicity. True, false or not enough information.Highlight 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 × Gplease give me step-by-step solution and circle answer please
- Draw the conjugate base for the acid CH,=CH,. Draw all hydrogens. Remember to include charges and non-bonding electrons where necessary. Select Draw Rings More Erase C HAde ed arrows to show the Arte attack the proton of the acid (breaking the X-H bond * Identify the nucleophile and electrophile ectants but the charge will be on a different molecule.) Circle the conjugate base. charges of any lons OK a) HO, b) кон SH c) NO. ONa HO + Approximate pK, values of Important organic functional groups pk, Protonated Cacborylic alcohol R. -2 5. 10 Phenol 16 Alcohol 25 Alkyne 38 Amine acid 44 Alkene 50 1. H OH R-OH R -H Alkane R. R. он R H ROH Protonated N amine H. H Thiol R-SHCurved 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 Arrows
- Highlight 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. H,N ОН OH ни Он OH x сComplete this mechanism for an acid-base reaction by adding curved arrows. H :0: H H Add/Remove step H H HO O olo ArConsider the structure of pyridine, a base. Modify the structure to draw the conjugate acid. Add or delete atoms, bonds, charges and non-bonding electrons where appropriate. Select Draw Rings More / C H N C Z Erase 2 Q
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