a.Give the curved arrow mechanism for the acid-base reaction, and the products.:0:+NaOH:O-H2-furoic acidb. Use a pKa table to determine the direction of equilibrium. Show the values you used above.so furnic acid

tion between 2-furoic acid and NaOH, the hydroxide ion (OH⁻) from NaOH will act as a base and…

Answered: a. Give the curved arrow mechanism for…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter5: Resonance

Section: Chapter Questions

Problem 13E: Complete each Lewis structure, draw all important resonance structures, predict a value for thebond...

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3. Give the pK₂ values for the following compounds and then rank them in terms of increasing acidity. Explain why the values change so dramatically (each pk- unit is an order of magnitude) from one member of the series to the next. H₂C=CH2 H₂C-CH₂ HC=CH
Ll.83.
Select the stronger base and then draw its conjugate acid below. CICH₂CH₂O or CH3CH₂O- • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • You do not have to include lone pairs in your answer. Ⓡ OO. n[1] ? ChemDoodle
Write a mechanism, using curved arrows, for the acid-base reaction given below. Show the correct structures for the products (including lone pair electrons). Label each component as acid, base, conjugate acid, and conjugate base. :o: H..: H-C
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1. Explain why the protonation of pyrrole occurs at C2 to form A, rather than the N atom to form B 2. Explain why compound A is more acidic than C, the conjugate acid of pyridine. :N-H H H H -H Pyrrole pKa=0.4 pKa=5.3 A B C H
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a. Give the curved arrow mechanism for the acid-base reaction, and the products. :0: + NaOH :O-H 2-furoic acid b. Use a pKa table to determine the direction of equilibrium. Show the values you used above. so furnic acid