No. Phenol is far more acidic than water.
why phenol more than aliphatic alcohol and water
Phenol is acidic in nature. The phenolate anion is stable through resonance. Hence, an acid base reaction ensues between phenol and NaOH in water resulting in the formation of sodium phenolate, which is highly soluble in water compared to phenol.
1-hexanol is an alcohol so it is a neutral compound not an acid while phenol is a strong acid.
Phenol can act as an acid due to it's stability as phenoxide ion. By releasing H+ ion it will form stable C6H5O- ion. The groups having +I, -I , +M , -M efffects present on phenol will effect acidic nature of phenol. As +I or +M groups which are present at ortho and at para psitions will decrease the acidic character of phenol. If they are at meta position effect is less than at para or ortho positions.Similar to this -I or -M gorups are substituted on phenol they will increase the acidic nature. so, we can say that as the stability of phenoxide ion increases acidic nature of phenol also increases.Phenol can act as an acid due to it's stability as phenoxide ion. By releasing H+ ion it will form stable C6H5O- ion. The groups having +I, -I , +M , -M efffects present on phenol will effect acidic nature of phenol. As +I or +M groups which are present at ortho and at para psitions will decrease the acidic character of phenol. If they are at meta position effect is less than at para or ortho positions.Similar to this -I or -M gorups are substituted on phenol they will increase the acidic nature. so, we can say that as the stability of phenoxide ion increases acidic nature of phenol also increases.Phenol is a weak acid because of the presence of the hydrogen ions.
Methanol is not acidic, it is not dissociable.
why phenol more than aliphatic alcohol and water
Phenol is acidic in nature. The phenolate anion is stable through resonance. Hence, an acid base reaction ensues between phenol and NaOH in water resulting in the formation of sodium phenolate, which is highly soluble in water compared to phenol.
Phenol. Anisole doesn't have any acidic protons.
phenol is more acidic because of the benzene ring present in the molecule,when you lose the H form the OH group it is possible to delocalise the charge around the aromatic system due to the pi electron cloud,straight chain alcohols cannot do this so it is less favourable to deprotonate them hance it is easier to deprotonate a phenol,hence we say it is more acidic
1-hexanol is an alcohol so it is a neutral compound not an acid while phenol is a strong acid.
Phenol can act as an acid due to it's stability as phenoxide ion. By releasing H+ ion it will form stable C6H5O- ion. The groups having +I, -I , +M , -M efffects present on phenol will effect acidic nature of phenol. As +I or +M groups which are present at ortho and at para psitions will decrease the acidic character of phenol. If they are at meta position effect is less than at para or ortho positions.Similar to this -I or -M gorups are substituted on phenol they will increase the acidic nature. so, we can say that as the stability of phenoxide ion increases acidic nature of phenol also increases.Phenol can act as an acid due to it's stability as phenoxide ion. By releasing H+ ion it will form stable C6H5O- ion. The groups having +I, -I , +M , -M efffects present on phenol will effect acidic nature of phenol. As +I or +M groups which are present at ortho and at para psitions will decrease the acidic character of phenol. If they are at meta position effect is less than at para or ortho positions.Similar to this -I or -M gorups are substituted on phenol they will increase the acidic nature. so, we can say that as the stability of phenoxide ion increases acidic nature of phenol also increases.Phenol is a weak acid because of the presence of the hydrogen ions.
Phenol solution, or phenol directly from the manufacturer?If the phenol is in the form it comes in from the factory, no chemical test is necessary. Phenol is a white crystalline solid.If it's dissolved in water, the easiest test is pH. Phenol solution is more acidic than ethanol. So...whatever you use for a pH test will do ya.
Methanol is not acidic, it is not dissociable.
in Cl the resonance occurs from 3p orbitals but in F resonance occurs from 2p orbitals due this reason F increase electron density in conjugate base more as compare to Cl .
Picric acid is 2,4,6-trinitro phenol, the nitro groups are electrons withdrawing groups so are responsible to make the bond weaker between oxygen and hydrogen atoms and increase the acidic strength as compare to phenol.
Phenol is more acidic than alcohols since the negative charge that is acquired by removal of a hydrogen atom can be delocalised into the molecules ring structure. acyclic alcohols cannot "spread" this charge as well as conjugated systems and thus will less readily lose their hydrogen atom.
Acidity depends on the concentration of H+. Due to higher electronegativity of sp2 hybridised carbon of phenol, the electron density on the oxygen decreases and hence increases the polarity O-H making the phenol unstable compared to phenolate, so it is more acidic. The C6H5-group is a fully sp2-hybridised electron pulling group.If you have electron providing groups (sp3) in CH3-CH2-O-H, it may decrease the polarity of O-H bond and destabilize the negatively charged ethanoate group (CH3CH2O-)