Phenol does not react with PCl5 under room temperature and pressure because the hydroxyl group (-OH) on phenol is not a strong enough nucleophile to displace the chloride ions in PCl5. Additionally, the lone pairs on the oxygen in phenol are occupied with electron delocalization within the benzene ring, making them less available for nucleophilic attack.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Phenol is not dissolved in a sodium hydroxide solution; having the characteristics of a weak acid phenol react with NaOH.
A positive Lucas test on phenol would indicate that phenol is a strong enough acid to react with Lucas reagent (a mixture of concentrated hydrochloric acid and zinc chloride) to form a cloudy solution or a precipitate. This reaction distinguishes phenol from other alcohols that do not react with the Lucas reagent.
The two compounds formed between PCl5 and ethanol are ethyl chloride (C2H5Cl) and diethyl ether (C4H10O). Ethyl chloride is produced when one mole of PCl5 reacts with one mole of ethanol, while diethyl ether is formed when two moles of ethanol react with one mole of PCl5.
Phenol does not react with PCl5 under room temperature and pressure because the hydroxyl group (-OH) on phenol is not a strong enough nucleophile to displace the chloride ions in PCl5. Additionally, the lone pairs on the oxygen in phenol are occupied with electron delocalization within the benzene ring, making them less available for nucleophilic attack.
Yes
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
what is the chemical equation when phenol react with hydrochloric acid
Phenol is not dissolved in a sodium hydroxide solution; having the characteristics of a weak acid phenol react with NaOH.
No, sodium bicarbonate will not react with phenol red. Phenol red is a pH indicator that changes color based on pH levels, while sodium bicarbonate is a salt commonly used as an antacid.
No they don't react together. but phenol is soluble in CHCl3.
A positive Lucas test on phenol would indicate that phenol is a strong enough acid to react with Lucas reagent (a mixture of concentrated hydrochloric acid and zinc chloride) to form a cloudy solution or a precipitate. This reaction distinguishes phenol from other alcohols that do not react with the Lucas reagent.
The two compounds formed between PCl5 and ethanol are ethyl chloride (C2H5Cl) and diethyl ether (C4H10O). Ethyl chloride is produced when one mole of PCl5 reacts with one mole of ethanol, while diethyl ether is formed when two moles of ethanol react with one mole of PCl5.
Phosphorus pentachloride (PCL5)
Para amino phenol can react with hydrochloric acid to form para-aminophenol hydrochloride salt. This reaction involves the protonation of the amino group on the para amino phenol molecule by the hydrochloric acid.
When Calcium chloride reacts with phenol red and baking soda, it will generate carbon dioxide gas. This reaction causes the phenol red to change color – it will turn from red to yellow as the pH decreases due to the formation of carbonic acid.