Alcohols, Phenols and Ethers
An unknown alcohol is treated with the 'Lucas reagent' to determine whether the alcohol is primary, secondary or tertiary. Which alcohol reacts fastest and by what mechanism?
Explain the following behavior: Reactivity of all the three classes of alcohols with conc. HCl and $$ZnCl_2$$ is different.
The reaction of alcohols with conc. HCl and Intakes place through the intermediate formation of carbonium ions. Greater the stability of carbonium ion greater is the reactivity of alcohol. Due to the +ve effect of alkyl groups, the stability of carbonium ion follows the order $$1^\circ<2^\circ<3^\circ$$. As a result of the reactivity of alcohol towards conc. HCI and $$ZnCl_2$$ follows the same order i.e.,
$$1^\circ<2^\circ<3^\circ$$
An unknown alcohol is treated with the 'Lucas reagent' to determine whether the alcohol is primary, secondary or tertiary. Which alcohol reacts fastest and by what mechanism?
From amongst the following alcohols the one that would react fastest with conc. $$HCl$$ and anhydrous $${Z}n{C}l_{2}$$, is:
An alcohol gave Lucas test in about 5 minutes. When the alcohol was treated with hot concentrated $$H_2SO_4$$, it gave an alkene of molecular formula $$C_4H_8$$ which on ozonolysis gives single product with molecular formula $$C_2H_4O$$. The structure of alcohol is:
Lucas test is given by an alcohol within 5 minutes. 0.22 g of which liberates 56 mL of $$ CH_4$$ at STP on treating with $$CH_3MgI$$.The structure of alcohol is:
Which of the following compounds reacts immediately with Lucas reagent?
Which alcohol will give immediate turbidity on shaking with HCl at room temperature?
An alcohol (A) gives Lucas test within 5 min. 7.4 g of alcohol when treated with sodium metal liberates 1120 mL of $$H_2$$ at STP. What will be alcohol (A)?
Which of the following alcohols reacts most readily with Lucas reagent?
Vinyl chloride and ethyl chloride can be distinguished by:
Which of the following will react fastest with Lucas reagent?