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प्रश्न
Write chemical equation of acetyl chloride with phenol
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उत्तर
संबंधित प्रश्न
Answer in one sentence/ word.
Write the IUPAC name of alcohol having molecular formula C4H10O which is resistant towards oxidation.
Oxidation of ethyl alcohol using K2Cr2O7/dil H2SO4 leads to formation of _______________
Arrange the following in decreasing order of acid strength.
CH3OH, CH3–CH2–OH, CH3–CH(OH)–CH3, (CH3)3–C–OH
Write the reaction to get aspirin from salicylic acid.
Draw intramolecular hydrogen bonding structure in o-nitrophenol.
How will you bring about the following conversions?
acetone to 2-methylpropan-2-ol
What is the action of conc. H2SO4 on carbolic acid at 373 K.
In the Lucas test for alcohols, the appearance of turbidity is due to the formation of ____________.
In phenols, −OH group is attached to ___________ hybridised carbon.
Phenol is obtained from cumene ____________.
The CORRECT decreasing order of boiling points for isomeric primary (1°), secondary (2°) and tertiary (3°) alcohols is ____________.
Phenol is ____________.
Isobutylene on hydroboration followed by oxidation with hydrogen peroxide in presence of base yields ______.
The number of isomeric alcohols possible with the formula C4H10O is ____________.
What is the product of the following reaction?
\[\ce{CH3 - CH2 - CH2 - OH ->[conc. H2SO4][\Delta]}\]
+I effect of alkyl groups in alcohols increases the stability of ____________.
____________ will NOT undergo acetylation.
Phenoxide ion is more stable than phenol due to the ____________.
Which of the following on oxidation yields ethyl methyl ketone?
Which of the following alcohols is NOT prepared by reduction of carbonyl compounds?
Which among the following phenolic compound is most acidic in nature?
The product C in the following reaction is
The order of reactivity of hydrogen halides with ether is as follows.
The major product obtained in the following reaction is
Write the product when 1°, 2° and 3° alcohol vapours are passed over hot copper.
Explain: Phenols are acid while alcohol is neutral.
What is the commercial method of preparation of phenol?
