Comparison of aciditiesComparing acidities of substituted and aromatic carboxylic acidsRationalizing Acidities of Ammonium Ion and Hydronium IonAcidities of amines and carboxylic acidsRelative acidities of alkanes, alkenes, and alkynesComparison Of Lewis AcidityBasicity comparison of halidesAcidities of (dimethylamino)acetophenone and (diphenylamino)acetophenoneComparison of acidic strength between nitric acid and nitrous acidDoes isopropyl chloride undergo SN1 or SN2 with sodium acetate?Order of Nucleophilicity
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Comparison of acidities
Comparing acidities of substituted and aromatic carboxylic acidsRationalizing Acidities of Ammonium Ion and Hydronium IonAcidities of amines and carboxylic acidsRelative acidities of alkanes, alkenes, and alkynesComparison Of Lewis AcidityBasicity comparison of halidesAcidities of (dimethylamino)acetophenone and (diphenylamino)acetophenoneComparison of acidic strength between nitric acid and nitrous acidDoes isopropyl chloride undergo SN1 or SN2 with sodium acetate?Order of Nucleophilicity
$begingroup$
My book says
To compare the acidities of two compounds, compare the stability of the anions formed by loss of a proton with respect to the original compound.
Suppose we have acetic acid and ethyl alcohol. Now on losing a proton, they form the respective anions:
My book again says
The acetate anion is resonance stabilized whereas in the ethoxide ion the charge is localized on the oxygen atom. Hence, acetate ion is more stable as compared to the ethoxide ion and hence, acetic acid is the stronger acid.
The problem is we have only compared the stabilities of the anions with respect to each other and not with respect to the original compounds. So how do we know that it is correct?
organic-chemistry acid-base
edited yesterday
Loong♦
34k884176
asked yesterday
StarboyStarboy
845
$endgroup$
add a comment |
$begingroup$
My book says
To compare the acidities of two compounds, compare the stability of the anions formed by loss of a proton with respect to the original compound.
Suppose we have acetic acid and ethyl alcohol. Now on losing a proton, they form the respective anions:
My book again says
The acetate anion is resonance stabilized whereas in the ethoxide ion the charge is localized on the oxygen atom. Hence, acetate ion is more stable as compared to the ethoxide ion and hence, acetic acid is the stronger acid.
The problem is we have only compared the stabilities of the anions with respect to each other and not with respect to the original compounds. So how do we know that it is correct?
organic-chemistry acid-base
edited yesterday
Loong♦
34k884176
asked yesterday
StarboyStarboy
845
$endgroup$
$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago
add a comment |
$begingroup$
My book says
To compare the acidities of two compounds, compare the stability of the anions formed by loss of a proton with respect to the original compound.
Suppose we have acetic acid and ethyl alcohol. Now on losing a proton, they form the respective anions:
My book again says
The acetate anion is resonance stabilized whereas in the ethoxide ion the charge is localized on the oxygen atom. Hence, acetate ion is more stable as compared to the ethoxide ion and hence, acetic acid is the stronger acid.
The problem is we have only compared the stabilities of the anions with respect to each other and not with respect to the original compounds. So how do we know that it is correct?
organic-chemistry acid-base
edited yesterday
Loong♦
34k884176
asked yesterday
StarboyStarboy
845
$endgroup$
My book says
To compare the acidities of two compounds, compare the stability of the anions formed by loss of a proton with respect to the original compound.
Suppose we have acetic acid and ethyl alcohol. Now on losing a proton, they form the respective anions:
My book again says
The acetate anion is resonance stabilized whereas in the ethoxide ion the charge is localized on the oxygen atom. Hence, acetate ion is more stable as compared to the ethoxide ion and hence, acetic acid is the stronger acid.
The problem is we have only compared the stabilities of the anions with respect to each other and not with respect to the original compounds. So how do we know that it is correct?
organic-chemistry acid-base
organic-chemistry acid-base
edited yesterday
Loong♦
34k884176
asked yesterday
StarboyStarboy
845
edited yesterday
Loong♦
34k884176
asked yesterday
StarboyStarboy
845
edited yesterday
Loong♦
34k884176
edited yesterday
Loong♦
34k884176
edited yesterday
Loong♦
34k884176
34k884176
asked yesterday
StarboyStarboy
845
asked yesterday
StarboyStarboy
845
asked yesterday
StarboyStarboy
845
845
$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago
add a comment |
$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago
$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago
$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago
add a comment |
1 Answer
1
active
oldest
votes
$begingroup$
Once you understand that the acetate ion is more stable the the ethoxide ion, we understand the fact that after releasing The acidic hydrogen the final product formed is more stable for acetic acid as compared to ethanol.
This would lead to the conclusion that acetic acid is a better acid as compared to ethanol.
While comparing the acidity of two species, only the comparative study of conjugate base is enough, since its simply the comparison between compounds.
Comparing the stability with the original compounds will lead you to the conclusion that whether the compound itself has a tendency to act as an acid or base.
Alternately one could compare the stability of the original compound and its conjugate(Which is the acid dissociation constant) and compare its value with the acid dissociation constant of other compunds to compare its acidity.
In any case comparing the stability of the conjugate ions will tell you which one of them is comparatively more acidic/basic than others. It will not let you conclude whether its the nature of the compound to naturally act as an acid/base or not. For that one should compare the stability with original compund or just check its dissociation constant.
answered yesterday
Sidharth GiriSidharth Giri
1368
$endgroup$
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
add a comment |
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1 Answer
1
active
oldest
votes
1 Answer
1
active
oldest
votes
active
oldest
votes
active
oldest
votes
$begingroup$
Once you understand that the acetate ion is more stable the the ethoxide ion, we understand the fact that after releasing The acidic hydrogen the final product formed is more stable for acetic acid as compared to ethanol.
This would lead to the conclusion that acetic acid is a better acid as compared to ethanol.
While comparing the acidity of two species, only the comparative study of conjugate base is enough, since its simply the comparison between compounds.
Comparing the stability with the original compounds will lead you to the conclusion that whether the compound itself has a tendency to act as an acid or base.
Alternately one could compare the stability of the original compound and its conjugate(Which is the acid dissociation constant) and compare its value with the acid dissociation constant of other compunds to compare its acidity.
In any case comparing the stability of the conjugate ions will tell you which one of them is comparatively more acidic/basic than others. It will not let you conclude whether its the nature of the compound to naturally act as an acid/base or not. For that one should compare the stability with original compund or just check its dissociation constant.
answered yesterday
Sidharth GiriSidharth Giri
1368
$endgroup$
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
add a comment |
$begingroup$
Once you understand that the acetate ion is more stable the the ethoxide ion, we understand the fact that after releasing The acidic hydrogen the final product formed is more stable for acetic acid as compared to ethanol.
This would lead to the conclusion that acetic acid is a better acid as compared to ethanol.
While comparing the acidity of two species, only the comparative study of conjugate base is enough, since its simply the comparison between compounds.
Comparing the stability with the original compounds will lead you to the conclusion that whether the compound itself has a tendency to act as an acid or base.
Alternately one could compare the stability of the original compound and its conjugate(Which is the acid dissociation constant) and compare its value with the acid dissociation constant of other compunds to compare its acidity.
In any case comparing the stability of the conjugate ions will tell you which one of them is comparatively more acidic/basic than others. It will not let you conclude whether its the nature of the compound to naturally act as an acid/base or not. For that one should compare the stability with original compund or just check its dissociation constant.
answered yesterday
Sidharth GiriSidharth Giri
1368
$endgroup$
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
add a comment |
$begingroup$
Once you understand that the acetate ion is more stable the the ethoxide ion, we understand the fact that after releasing The acidic hydrogen the final product formed is more stable for acetic acid as compared to ethanol.
This would lead to the conclusion that acetic acid is a better acid as compared to ethanol.
While comparing the acidity of two species, only the comparative study of conjugate base is enough, since its simply the comparison between compounds.
Comparing the stability with the original compounds will lead you to the conclusion that whether the compound itself has a tendency to act as an acid or base.
Alternately one could compare the stability of the original compound and its conjugate(Which is the acid dissociation constant) and compare its value with the acid dissociation constant of other compunds to compare its acidity.
In any case comparing the stability of the conjugate ions will tell you which one of them is comparatively more acidic/basic than others. It will not let you conclude whether its the nature of the compound to naturally act as an acid/base or not. For that one should compare the stability with original compund or just check its dissociation constant.
answered yesterday
Sidharth GiriSidharth Giri
1368
$endgroup$
Once you understand that the acetate ion is more stable the the ethoxide ion, we understand the fact that after releasing The acidic hydrogen the final product formed is more stable for acetic acid as compared to ethanol.
This would lead to the conclusion that acetic acid is a better acid as compared to ethanol.
While comparing the acidity of two species, only the comparative study of conjugate base is enough, since its simply the comparison between compounds.
Comparing the stability with the original compounds will lead you to the conclusion that whether the compound itself has a tendency to act as an acid or base.
Alternately one could compare the stability of the original compound and its conjugate(Which is the acid dissociation constant) and compare its value with the acid dissociation constant of other compunds to compare its acidity.
In any case comparing the stability of the conjugate ions will tell you which one of them is comparatively more acidic/basic than others. It will not let you conclude whether its the nature of the compound to naturally act as an acid/base or not. For that one should compare the stability with original compund or just check its dissociation constant.
answered yesterday
Sidharth GiriSidharth Giri
1368
edited yesterday
answered yesterday
Sidharth GiriSidharth Giri
1368
answered yesterday
Sidharth GiriSidharth Giri
1368
answered yesterday
Sidharth GiriSidharth Giri
1368
1368
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
add a comment |
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
2
2
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
$begingroup$
Just sthg that I would like to quip here: The answerer has not explicitly mentioned why comparing stabilities of an acid and it's conjugate base gives it's acidic/basic nature. This is because we consider acidity-basicity when a dynamic equilibrium exists b/w an acid and it's Brönsted base... And here,the reaction is driven towards that side where lower Gibbs free energy is available, or which side is more thermodynamically "stable". The arguments stated above would not work at any other reaction coordinate where kinetics would be the governing factor. Otherwise, +1
$endgroup$
– YUSUF HASAN
yesterday
add a comment |
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$begingroup$
Comparing basicities does give you information about related acidities.
$endgroup$
– Mithoron
23 hours ago