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- 6. Consider the following acid/base reaction. OH a) Show an arrow pushing mechanism. b) Calculate Keq. H CNA -07. For each draw the mechanism (using arrows) and label acid, base, conjugate acid, conjugate base :0: NH3 :OH H,ö:rank these compounds in order of increasing basicity Rank these compounds in order of increasing basicity (most basic at the bottom). C A B G Drag and drop options into correct order and submit. A too B FF |||
- Rank the indicated a-H’s from most to least acidic (most acidic= 1). Be sure to explain your rankings for each by drawing significant resonance structures for the conjugate base and commenting on any other factors that contribute to your rankings.INSTRUCTION: Complete the reaction map by matching A-E with the given choices. H2 H2 A B E Na in lig NH3 Pt D OH + HO/ Match each item to a choice Choices: NaBH, Hyo KMO.Answer first 3 please ( a-c)
- For each of these molecules, draw in the most acidic protons and rank the molecules from most acidic to least acidic. ·FO Attempt 1 Draw curved arrows to illustrate the Bnsted acid-base reaction shown. H3C H3C c=CH2 + H-Br: +C- CH2 + :Br H3C H3C H. Draw the curved arrows for the forward reaction. Draw the curved arrows for the reverse reaction. H,C H,C C= CH, H Br : H,C H,C MacBook Air1. For each set of reagents below: i) Predict the products of a single acid-base reaction. ii) Draw the electron-pushing mechanism of the acid-base reaction using curved arrows. iii) Identify the acid, base, conjugate acid, and conjugate base iv) Predict whether the reaction favors the reactants or the products. a) NH3 + HCl → b) CH3CH₂CO₂H + NaCH₂CH3 c) NaOCH3 + H₂O → d) CH3C=CNa + H₂SO4 → e) NaNH2+ HF
- Click on a basic (nucleophilic) atom. HH | | H-C-C=C₂ | H H H H-CI:3. 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 요left 4. Consider the following equilibrium: 29925610 + Aga weak and Sung base Bast CORS + 1ght base: Strong ad d AddOH ress stable OH Is the carboxylate anion (CH3CH₂COO) an appropriate base to deprotonate the alcohol? A) yes, because the equilibrium favors the left side B) yes, because the equilibrium favors the right side C) no, because the equilibrium favors the left side D) no, because the equilibrium favors the right side OH COO bas