The most acidic proton on the molecule below has pK 41. Which of the following bases are capable of deprotonating the proton? Check all that apply. Note: Reference the pK of selected organic compounds table for additional information. Acid CH₂CH₂OH 16 H₂CO3 6.4 H₂O H₂ C₂H10 O NaH pk value NaHCO3 O NaOH 14 □ NaOCH₂ CH3 35 50 □ BuLi (C₂H₂Li) None of the above X

The most acidic proton on the molecule below has pK 41. Which of the following bases are capable of deprotonating the proton? Check all that apply. Note: Reference the pK of selected organic compounds table for additional information. Acid CH₂CH₂OH 16 H₂CO3 6.4 H₂O H₂ C₂H10 O NaH pk value NaHCO3 O NaOH 14 □ NaOCH₂ CH3 35 50 □ BuLi (C₂H₂Li) None of the above X

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter20: Carboxylic Acids And Nitriles

Section20.3: Biological Acids And The Henderson–hasselbalch Equation

Problem 5P: Calculate the percentages of dissociated and undissociated forms present in the following solutions:...

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Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.

Question

The most acidic proton on the molecule below has pKa 41. Which of the following bases are capable of deprotonating the proton? Check all that apply.

The most acidic proton on the molecule below has pK 41. Which of the following bases are capable of deprotonating the proton? Check all that apply.
a
Note: Reference the pK of selected organic compounds table for additional information.
Acid
CH3CH₂OH 16
H₂CO3
H₂O
H₂
C₂H10
O NaH
pk value
a
□ NaHCO3
□ NaOH
6.4
14
NaOCH₂CH₂
35
50
□ BuLi (C₂H₂Li)
None of the above
X
G

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