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

Chapter13: Substitution

Section: Chapter Questions

Problem 29CTQ

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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
a. Explain why protonation of pyrrole occurs at C2 to form A, rather than on the N atom to form B. b. Explain why A is more acidic than C, the conjugate acid of pyridine.
Draw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. HCI Drawing C:O
Hw.42.
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
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
11
Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. :0: NaOH Drawing D
None
4. Using curved arrows, draw a reaction mechanism and predict the products. Lewis Acid-Base Reaction of a) :: Bronsted Acid-Base Reaction b) P. + AICI3
Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. A table of pka values for various organic and inorganic acids can be found in the references section. ata CH3 CH3 -CH3 CH3 CH,- в D ethoxide ethanol dimethylsulfone anion dimethylsulfone a) The weaker base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. AC)

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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