Benzyl alcohol anisole phenol how to distinguish
1. density and solubility analysis
benzyl alcohol
- Density: about 0.95g/cm³
- Solubility: Slightly soluble in water, but easily with ethanol
- Physical: Colorless liquid, with a slight sour taste
benzyl ether
- Density: about 0.73g/cm³
- Solubility: Slightly soluble in water, soluble in organic solvents
- Physical properties: colorless liquid, odorless and harmless
phenol
- Density: about 1.01g/cm³
- Solubility: Slightly soluble in water, but soluble in ethanol
- Physical properties: colorless liquid, tasteless slightly acidic
By comparing the density and solubility, the three compounds can be initially distinguished. The density of benzyl alcohol is slightly greater than that of anisole, while the density of phenol is slightly higher than that of both.
2. structure chemical properties comparison
benzyl alcohol
- Structure: The benzene ring is connected to an ethanol group (-CH2OH)
- Chemical: easy hydrolysis, and alkaline conditions in the neutralization reaction
benzyl ether
- Structure: Benzene ring linked to a methoxy (-CH2O)
- Chemical: stability is better, in acidic conditions more stable, but in strong alkali or light conditions will occur hydrolysis
phenol
- Structure: Benzene ring directly connected to a hydroxyl group (-OH)
- Chemical: acidic, easy hydrolysis, and in the catalyst with sulfuric acid reaction to produce phenol sulfuric acid
From the structural point of view, these three compounds are derivatives of benzene ring, but the position and connection of hydroxyl groups are different, resulting in significant differences in their chemical properties.
3. chemical reaction characteristics
hydrolysis reaction
- Benzyl alcohol: in alkaline conditions will occur hydrolysis reaction, the formation of sodium benzoate and ethanol.
- Anisole: no hydrolysis reaction, chemical stability.
- Phenol: in alkaline conditions will occur hydrolysis reaction, generate sodium phenolate.
with acid-base reaction
- Benzyl alcohol: with alkaline substances in the neutralization reaction, the formation of benzoate.
- Anisole: does not react with acid and alkali.
- Phenol: and alkaline substances in the neutralization reaction, generating the corresponding phenol salt.
catalytic reaction
- Benzyl alcohol: in the catalyst, can be with other substances in addition or substitution reaction.
- Anisole: chemical stability is high, does not occur such reactions.
- Phenol: in the catalyst, can react with sulfuric acid to generate phenol sulfuric acid.
These three compounds can be further separated by chemical reaction characteristics. Both benzyl alcohol and phenol have strong acid-base reactivity, but the hydrolysis of benzyl alcohol under alkaline conditions is more significant.
, 4. practical application of the distinction method
In practical applications, the distinction between these three compounds can be achieved:
- Density and solubility experiment
- Measurement of three compounds density, combined with solubility test for preliminary discrimination.
- The mixture was ground and separated to observe the dissolution.
- chemical reaction experiment
- Test three compounds in acidic or basic conditions of the reaction characteristics, observe whether there is obvious hydrolysis reaction or neutralization reaction.
- In the presence of a catalyst, it is tested whether an addition or substitution reaction can occur.
- molecular structure analysis
- Through instrumental analysis (such as infrared spectroscopy, nuclear magnetic resonance, etc.) to further confirm the molecular structure, so as to achieve accurate distinction.
5. summary
Although benzyl alcohol, anisole and phenol are all derivatives of benzene, they have significant differences due to their different structures and chemical properties. Through the analysis of density, solubility, structure and chemical reaction, these three compounds can be accurately distinguished. In practical applications, the combination of experimental methods and instrumental analysis can efficiently achieve their distinction. Mastering the differences between these three compounds will not only help improve the efficiency of chemical production, but also make greater contributions to environmental protection and safety.
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