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.
Hydrochloric acid is more acidic than picric acid. Hydrochloric acid fully dissociates in solution to release hydrogen ions, resulting in a lower pH compared to picric acid, which is a weaker acid that does not fully dissociate in solution.
Picric acid is a fairly strong acid. Most phenols are very weak acids, although they do react with strong bases. Since picric acid (2,4,6-trinitrophenol) has three strong electron-withdrawing nitro groups on its ring, its anion is more stable than most phenolates, and that makes it a much stronger acid.
Phenol is more acidic than 1-hexanol because the hydroxyl group in phenol is directly attached to the aromatic ring, which stabilizes the resulting phenoxide ion through resonance. In contrast, the hydroxyl group in 1-hexanol is attached to an aliphatic chain, making it less acidic.
The two resonating structure of the anion formed after acetic acid gives up a proton are equivalent, and the negative charge rests on oxygen which is an electronegative element. But in case of phenoxide ion, the resonating structures are not equivalent, and negative charge rests on carbon which is an electropositive atom.
No, water is neutral with a pH of 7. Phenol is slightly acidic with a pH range between 5 and 6.
Hydrochloric acid is more acidic than picric acid. Hydrochloric acid fully dissociates in solution to release hydrogen ions, resulting in a lower pH compared to picric acid, which is a weaker acid that does not fully dissociate in solution.
picric acid (or 2,4,6-trinitrophenol) is more acidic than benzoic acid The pKa or picric acid is 0.3 and that of benzoic acid is 4.2
Picric acid is a fairly strong acid. Most phenols are very weak acids, although they do react with strong bases. Since picric acid (2,4,6-trinitrophenol) has three strong electron-withdrawing nitro groups on its ring, its anion is more stable than most phenolates, and that makes it a much stronger acid.
Phenol is more acidic than 1-hexanol because the hydroxyl group in phenol is directly attached to the aromatic ring, which stabilizes the resulting phenoxide ion through resonance. In contrast, the hydroxyl group in 1-hexanol is attached to an aliphatic chain, making it less acidic.
The two resonating structure of the anion formed after acetic acid gives up a proton are equivalent, and the negative charge rests on oxygen which is an electronegative element. But in case of phenoxide ion, the resonating structures are not equivalent, and negative charge rests on carbon which is an electropositive atom.
No, water is neutral with a pH of 7. Phenol is slightly acidic with a pH range between 5 and 6.
Phenol. Anisole doesn't have any acidic protons.
C6H5OH is considered acidic. It is more commonly known as phenol, or carbolic acid, which is a type of organic solid known for its volatility and crystalline structure.
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
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.
No, it isn't. It's essentially neutral. Some alcohols are weakly acidic... phenol is one of the more acidic ones, and was at one time even called "carbolic acid."
Phenol is more acidic because cresol has +I effect of CH3 grup as you know acidity is reciprocal of +I effect. OR Cresol has electron donating methyl group, whih reduces its electron defficiency of the phenol group and hence acidity.