The comparison of acidic strength of the given acids has to be done by using their given pK a values. Concept introduction: In aqueous solution an acid undergoes ionization. The ionization of an acid is can be expressed in terms of equilibrium constant. The quantitative measurement tells about the strength of the acid. Higher the value of K a stronger will be the acid. The acid dissocition can be represented as following equilibrium, HA ( aq ) + H 2 O ( l ) ⇌ H 3 O + ( aq ) + A − 1 ( aq ) The dissociation constant for the acid is K a , K a = [ H 3 O + ] [ A − ] [ HA ] For simplifications, pK a value is used to find the acidic strength of acid which is calculated by taking negative logarithm of K a . pK a = − log ( K a ) The lower value of pK a of an acid, stronger will be the acid. Thus on comparing the pK a value it can be determined which acid is stronger one among them.
The comparison of acidic strength of the given acids has to be done by using their given pK a values. Concept introduction: In aqueous solution an acid undergoes ionization. The ionization of an acid is can be expressed in terms of equilibrium constant. The quantitative measurement tells about the strength of the acid. Higher the value of K a stronger will be the acid. The acid dissocition can be represented as following equilibrium, HA ( aq ) + H 2 O ( l ) ⇌ H 3 O + ( aq ) + A − 1 ( aq ) The dissociation constant for the acid is K a , K a = [ H 3 O + ] [ A − ] [ HA ] For simplifications, pK a value is used to find the acidic strength of acid which is calculated by taking negative logarithm of K a . pK a = − log ( K a ) The lower value of pK a of an acid, stronger will be the acid. Thus on comparing the pK a value it can be determined which acid is stronger one among them.
Solution Summary: The author explains that the ionization of an acid is expressed in terms of equilibrium constant. The acid dissociation constant is pK_a.
Interpretation: The comparison of acidic strength of the given acids has to be done by using their given pKa values.
Concept introduction: In aqueous solution an acid undergoes ionization. The ionization of an acid is can be expressed in terms of equilibrium constant. The quantitative measurement tells about the strength of the acid. Higher the value of Ka stronger will be the acid. The acid dissocition can be represented as following equilibrium,
HA(aq)+ H2O(l)⇌ H3O+(aq)+ A−1(aq)
The dissociation constant for the acid is Ka,
Ka=[H3O+][A−][HA]
For simplifications, pKa value is used to find the acidic strength of acid which is calculated by taking negative logarithm of Ka.
pKa=−log(Ka)
The lower value of pKa of an acid, stronger will be the acid. Thus on comparing the pKa value it can be determined which acid is stronger one among them.
Draw the Fischer projection of D-fructose.
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Consider this step in a radical reaction:
Y
What type of step is this? Check all that apply.
Draw the products of the step on the right-hand side of the drawing area
below. If more than one set of products is possible, draw any set.
Also, draw the mechanism arrows on the left-hand side of the drawing
area to show how this happens.
ionization
propagation
initialization
passivation
none of the above
22.16 The following groups are ortho-para directors.
(a)
-C=CH₂
H
(d)
-Br
(b)
-NH2
(c)
-OCHS
Draw a contributing structure for the resonance-stabilized cation formed during elec-
trophilic aromatic substitution that shows the role of each group in stabilizing the
intermediate by further delocalizing its positive charge.
22.17 Predict the major product or products from treatment of each compound with
Cl₁/FeCl₂-
OH
(b)
NO2
CHO
22.18 How do you account for the fact that phenyl acetate is less reactive toward electro-
philic aromatic substitution than anisole?
Phenyl acetate
Anisole
CH
(d)
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