Don't use AI O-HNaOHInitially formedThis anion rapidly undergoes an intramolecular proton transfer, in which the negatively charged oxygen atom abstracts the nearbyacidic proton.Draw the curved arrows showing a proton transfer reaction, and modify the given structure to draw the product of that protontransfer. Lone pairs are not required in the product.-H-Ö:Edit DrawingOH

Answered: Image /qna-images/answer/32a31654-0816-4a19-9cf9-309aaa4bb3dc.jpg

Answered: O-H NaOH Initially formed This anion…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter4: Polar Bonds, Polar Reactions

Section: Chapter Questions

Problem 23E: Summarize the relationship between pKa and acid strength by completing the following sentences: a....

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For the following reaction identify the acid and the base and predict the products. Draw the curved arrow mechar II Identify the acid and the base: acid base Draw the curved arrow mechanism for the formation of products. Include Lone Pairs in your answer. ? Edit Predict the direction of the equilibrium. Equilibrium will favor the yof the reaction.
O 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 Air
H₂C H₂C لیے CH–COOH +CH,CH(CH,)NH, H₂C heat 2 Reaction D Select Draw Rings More Erase / |||||| CON H COOH +CH,CH(CH,)NH₂ CH3 Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. heat G Q2Q
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).
Draw the major product Only typed solution
r Please don't provide handwritten solution
Complete the following reaction:
Using ChemDraw Draw a mechanism of a reversible reaction of acetophenone and strong acid (H-A) to form a protonated acetophenone and a weak base. Draw all the electron pairs of the molecules and the arrows.
Draw the curved arrows showing a proton transfer reaction, and draw the products of that proton transfer. Do not include the Li+ counterion, and lone pairs are not required in the products. H₂C CH₂ + H—B—H
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Rank the bold-faced hydrogens for the following compounds from most acidic to least acidic. Ho I ||| > IV > I > V > || || > ||| > V > IV > | || > V > ||| > IV > | O V > III > II > IV > | O III > I > IV > V > || I H //ICH3 H III IV OH H V
Rank the bold-faced hydrogens for the following compounds from most acidic to least acidic. The table below can be useful to answer this problem. I Short pka table Functional group Hydrochloric acid Carboxylic acids Protonated amines Water Alkyne Amine Alkane OII>IV> V> ||| > | OIV>II>I>V > III OV> III > IV> II > I II CI co₂H Stronger Example acid pka HCI: H3C NHÀ :C HO-H H3C-CEC-H : NH3 III CH4 Weaker acid -8 5 10 14 25 -35 ~50 IV CO₂H conj. base :CI: H₂C : NH3 e.. : OH R-CEC: : NH₂ CH3 V Weaker base Stronger base H

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