Consider all steps and intermediates. Which of the following is a correct statement?
- ANucleophilic addition
- BNucleophilic substitution reaction
- CProduct obtained is chiral
- DAll
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Similar Questions
In which one of the following conversions is phosphorus pentachloride $(PCl_5)$ used as a reagent?
Medium
View SolutionMatch the following:
Column-$I$: Compound / Reagent Column-$II$: Other name / Chemical / Process $A$. Methanol $I$. Lucas reagent $B$. $ZnCl_2$ / Conc. $HCl$ $II$. Baeyer's reagent $C$. Rectified spirit $III$. Wood spirit $D$. Dil. $KMnO_4$ $IV$. $95 \% C_2H_5OH$ - $V$. $75 \% C_2H_5OH$ - $VI$. $90 \% C_3H_7OH$
The correct match is:
| Column-$I$: Compound / Reagent | Column-$II$: Other name / Chemical / Process |
|---|---|
| $A$. Methanol | $I$. Lucas reagent |
| $B$. $ZnCl_2$ / Conc. $HCl$ | $II$. Baeyer's reagent |
| $C$. Rectified spirit | $III$. Wood spirit |
| $D$. Dil. $KMnO_4$ | $IV$. $95 \% C_2H_5OH$ |
| - | $V$. $75 \% C_2H_5OH$ |
| - | $VI$. $90 \% C_3H_7OH$ |
The correct match is:
DifficultTS EAMCET 2021
View SolutionMatch the reactions given in Column-$I$ with the names of the products and reactions given in Column-$II$.
Column-$I$ (Reaction) Column-$II$ (Product and Reaction Name) $A$. Phenol $+$ dilute $HNO_3$ $i$. Mononitrophenol,Nitration $B$. Phenol $+$ Bromine water $ii$. $2,4,6$-Tribromophenol,Bromination $C$. Phenol $+$ $Na_2Cr_2O_7/H_2SO_4$ $iii$. Benzoquinone,Oxidation $D$. Sodium phenoxide $+$ $CO_2$ followed by $H^+$ $iv$. Salicylic acid,Kolbe reaction
| Column-$I$ (Reaction) | Column-$II$ (Product and Reaction Name) |
| $A$. Phenol $+$ dilute $HNO_3$ | $i$. Mononitrophenol,Nitration |
| $B$. Phenol $+$ Bromine water | $ii$. $2,4,6$-Tribromophenol,Bromination |
| $C$. Phenol $+$ $Na_2Cr_2O_7/H_2SO_4$ | $iii$. Benzoquinone,Oxidation |
| $D$. Sodium phenoxide $+$ $CO_2$ followed by $H^+$ | $iv$. Salicylic acid,Kolbe reaction |
Medium
View SolutionWhich of the following statements is not correct?
Difficult
View SolutionMatch the common names of the ethers given in Column $(I)$ with their structures in Column $(II)$ and their $\text{IUPAC}$ names in Column $(III)$.
Column $(I)$ Column $(II)$ Column $(III)$ $(A)$ Methyl isopropyl ether $(1)$ ${C_6}{H_5}O{(CH_2)_6}CH_3$ $(i)$ $2$-Methoxypropane $(B)$ Phenyl isopentyl ether $(2)$ $CH_3-O-CH(CH_3)_2$ $(ii)$ Methoxyethane $(C)$ Heptyl phenyl ether $(3)$ ${C_6}{H_5}-O-CH_2CH_2CH(CH_3)_2$ $(iii)$ $1$-Phenoxyheptane $(D)$ Ethyl methyl ether $(4)$ $CH_3CH_2-O-CH_3$ $(iv)$ $1$-Methoxy$-3-$methylbutane (or $3$-Methylbutoxybenzene)
| Column $(I)$ | Column $(II)$ | Column $(III)$ |
|---|---|---|
| $(A)$ Methyl isopropyl ether | $(1)$ ${C_6}{H_5}O{(CH_2)_6}CH_3$ | $(i)$ $2$-Methoxypropane |
| $(B)$ Phenyl isopentyl ether | $(2)$ $CH_3-O-CH(CH_3)_2$ | $(ii)$ Methoxyethane |
| $(C)$ Heptyl phenyl ether | $(3)$ ${C_6}{H_5}-O-CH_2CH_2CH(CH_3)_2$ | $(iii)$ $1$-Phenoxyheptane |
| $(D)$ Ethyl methyl ether | $(4)$ $CH_3CH_2-O-CH_3$ | $(iv)$ $1$-Methoxy$-3-$methylbutane (or $3$-Methylbutoxybenzene) |
Medium
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