Phenol. Anisole doesn't have any acidic protons.
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 .
Phenol is a weak acid, so it can turn blue litmus paper red, indicating its acidic nature. However, phenol does not significantly affect red litmus paper, as it is not a strong enough acid to change its color. Overall, phenol primarily affects blue litmus paper by turning it red.
Very strong acid solutions that have phenolphthalein added to them turn orange, but in general acidic solutions with phenolphthalein are colorless. If the solution is titrated to slightly basic (pH > 8.2) it will turn pink. Note that in extremely basic solutions (pH > 13) it will revert to colorless again.
Anisole can be converted into phenol by using a strong aqueous acid, such as hydrochloric acid, in the presence of water and heat. The acidic conditions will cleave the methoxy group (–OCH3) from the benzene ring, resulting in the formation of phenol. This reaction is known as hydrolysis of an ether.
A strong acid is typically stronger than phenol in terms of acidity due to its ability to fully dissociate in water to release protons. Phenol is a weak acid that only partially dissociates in water, making it less acidic compared to strong acids like hydrochloric acid or sulfuric acid.
No, water is neutral with a pH of 7. Phenol is slightly acidic with a pH range between 5 and 6.
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
p-chloro phenol is more acidic thisi is because in p-fluoro phenol as fluorine and carbon have identical 2p orbitals, the overlapping is perfect Hence the +r effect and -I effect cancels thus making it less acidic
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.
Phenol and benzene are both aromatic compounds, but phenol has a hydroxyl group (-OH) attached to the benzene ring, making it more reactive than benzene. Phenol can undergo reactions such as oxidation and substitution more readily than benzene. Additionally, phenol is more acidic than benzene due to the presence of the hydroxyl group.
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 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 is stronger acid than ethanol. Phenol's acidic strength stems from the presence of the -OH group attached directly to the aromatic ring, which allows it to readily donate a proton. Ethanol, in contrast, has a less acidic -OH group due to its aliphatic structure.
Normal ferric chloride gives a positive test for phenol as it forms a violet complex with it. This can lead to false positives in other compounds that also react with ferric chloride, making it unreliable for detecting phenol specifically. Instead, a modified version called FeCl3/KI reagent is commonly used for phenol detection as it gives a distinct green color with phenol, allowing for more accurate and specific results.
Phenol is more acidic than aliphatic alcohols and water because the benzene ring stabilizes the phenoxide ion formed upon deprotonation, making it more favorable to lose a proton. This stabilization is due to resonance delocalization of the negative charge in the phenoxide ion. In aliphatic alcohols and water, there is no such resonance stabilization, resulting in weaker acidity.
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.
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.