Which of the following bases are strong enough to deprotonate CH 3 CH 2 CH 2 C ≡ CH ( p K a = 25 ) , so that equilibrium favors the products: (a) H 2 O ; (b) NaOH ; (c) NaNH 2 ; (d) NH 3 ; (e) NaH ; (f) CH 3 Li ?
Which of the following bases are strong enough to deprotonate CH 3 CH 2 CH 2 C ≡ CH ( p K a = 25 ) , so that equilibrium favors the products: (a) H 2 O ; (b) NaOH ; (c) NaNH 2 ; (d) NH 3 ; (e) NaH ; (f) CH 3 Li ?
Solution Summary: The author explains the Bronsted-Lowry theory that when an acid donates a proton, the species formed is known as conjugate acid.
Which of the following bases are strong enough to deprotonate
CH
3
CH
2
CH
2
C
≡
CH
(
p
K
a
=
25
)
, so that equilibrium favors the products: (a)
H
2
O
; (b)
NaOH
; (c)
NaNH
2
; (d)
NH
3
; (e)
NaH
; (f)
CH
3
Li
?
Which of the following bases are strong enough to deprotonate C6H5OH (pKa = 10) so that equilibrium favors the products: (a) H2O; (b) NaOH; (c) NaNH2; (d) CH3NH2; (e) NaHCO3; (f) NaSH; (g) NaH?
Which of the following bases are strong enough to deprotonate C6H5OH(pKa = 10) so that equilibrium favors the products:(a) H2O; (b) NaOH; (c) NaNH2; (d) CH3NH2; (e) NaHCO3; (f) NaSH; (g)NaH?
For the following reactions, predict the likely product(s) of the reaction or write 'no reaction."
Me
H
Me
°x
Me
Me
Me
Br
Me
Me
Me
Nal, NaOCI
EtOH, H₂O
HNO3
ACOH
AICI 3
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