-
question_answer1)
Ethanol is prepared industrially by [MP PMT 1989]
A)
Hydration of ethylene done
clear
B)
Fermentation of sugars done
clear
C)
Both the above done
clear
D)
None of these done
clear
View Solution play_arrow
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question_answer2)
Ethyl alcohol is industrially prepared from ethylene by [CPMT 1985]
A)
Permanganate oxidation done
clear
B)
Catalytic reduction done
clear
C)
Absorbing in \[{{H}_{2}}S{{O}_{4}}\] followed by hydrolysis done
clear
D)
Fermentation done
clear
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question_answer3)
Propene, \[C{{H}_{3}}-CH=C{{H}_{2}}\] can be converted to 1-propanol by oxidation. Which set of reagents among the following is ideal to effect the conversion [CBSE PMT 1991]
A)
Alkaline \[KMn{{O}_{4}}\] done
clear
B)
\[{{B}_{2}}{{H}_{6}}\] and alkaline \[{{H}_{2}}{{O}_{2}}\] done
clear
C)
\[{{O}_{3}}/Zn\] dust done
clear
D)
\[Os{{O}_{4}}/C{{H}_{4}},C{{l}_{2}}\] done
clear
View Solution play_arrow
-
question_answer4)
Which one of the following will produce a primary alcohol by reacting with \[C{{H}_{3}}MgI\] [MP PET 1991]
A)
Acetone done
clear
B)
Methyl cyanide done
clear
C)
Ethylene oxide done
clear
D)
Ethyl acetate done
clear
View Solution play_arrow
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question_answer5)
The fermentation of starch to give alcohol occurs mainly with the help of [CPMT 1971; MH CET 1999; RPMT 2000]
A)
\[{{O}_{2}}\] done
clear
B)
Air done
clear
C)
\[C{{O}_{2}}\] done
clear
D)
Enzymes done
clear
View Solution play_arrow
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question_answer6)
Coconut oil upon alkaline hydrolysis gives [MP PET 1991; AFMC 2000; KCET 2001; BCECE 2005]
A)
Glycol done
clear
B)
Alcohol done
clear
C)
Glycerol done
clear
D)
Ethylene oxide done
clear
View Solution play_arrow
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question_answer7)
Which enzyme converts glucose and fructose both into ethanol [MP PMT 1989, 90, 96; CPMT 1983, 84, 86, 94; KCET 1989; MNR 1978; MP PET 1994, 99]
A)
Diastase done
clear
B)
Invertase done
clear
C)
Zymase done
clear
D)
Maltase done
clear
View Solution play_arrow
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question_answer8)
Chlorination of toluene in the presence of light and heat followed by treatment with aqueous NaOH gives [IIT-JEE 1990]
A)
o-cresol done
clear
B)
p-cresol done
clear
C)
2, 4-dihydroxy toluene done
clear
D)
Benzyl alcohol done
clear
View Solution play_arrow
-
question_answer9)
In the commercial manufacture of ethyl alcohol from starchy substances by fermentation method, which enzymes stepwise complete the fermentation reaction [BIT 1992]
A)
Diastase, maltase and zymase done
clear
B)
Maltase, zymase and invertase done
clear
C)
Diastase, zymase and lactase done
clear
D)
Diastase, invertase and zymase done
clear
View Solution play_arrow
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question_answer10)
Primary alcohols can be obtained from the reaction of the RMgX with [Pb. PMT 2001]
A)
\[C{{O}_{2}}\] done
clear
B)
\[HCHO\] done
clear
C)
\[C{{H}_{3}}CHO\] done
clear
D)
\[{{H}_{2}}O\] done
clear
View Solution play_arrow
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question_answer11)
On heating aqueous solution of benzene diazonium chloride, which is formed [CPMT 1988; BHU 1980]
A)
Benzene done
clear
B)
Chlorobenzene done
clear
C)
Phenol done
clear
D)
Aniline done
clear
View Solution play_arrow
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question_answer12)
\[LiAl{{H}_{4}}\] converts acetic acid into [CPMT 1977; MP PMT 1990, 92]
A)
Acetaldehyde done
clear
B)
Methane done
clear
C)
Ethyl alcohol done
clear
D)
Methyl alcohol done
clear
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question_answer13)
Formaldehyde gives an additive product with methyl magnesium iodide which on aqueous hydrolysis gives [MP PMT/PET 1988]
A)
Isopropyl alcohol done
clear
B)
Ethyl alcohol done
clear
C)
Methyl alcohol done
clear
D)
Propyl alcohol done
clear
View Solution play_arrow
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question_answer14)
Benzyl alcohol is obtained from benzaldehyde by [CPMT 1983; MNR 1993]
A)
Fittig's reaction done
clear
B)
Cannizaro's reaction done
clear
C)
Kolbe's reaction done
clear
D)
Wurtz's reaction done
clear
View Solution play_arrow
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question_answer15)
Benzene diazonium chloride on boiling with dilute sulphuric acid gives [MP PMT 1983]
A)
Toluene done
clear
B)
Benzoic acid done
clear
C)
Benzene done
clear
D)
Phenol done
clear
View Solution play_arrow
-
question_answer16)
The reaction given below is known as \[{{C}_{2}}{{H}_{5}}ONa+I{{C}_{2}}{{H}_{5}}\xrightarrow{{}}{{C}_{2}}{{H}_{5}}O{{C}_{2}}{{H}_{5}}+NaI\] [CPMT 1990; KCET 1990; MH CET 2003; Pb. CET 2002]
A)
Kolbe's synthesis done
clear
B)
Wurtz's synthesis done
clear
C)
Williamson's synthesis done
clear
D)
Grignard's synthesis done
clear
View Solution play_arrow
-
question_answer17)
Salicylaldehyde can be prepared from [CPMT 1983]
A)
Phenol and chloroform done
clear
B)
Phenol, chloroform and sodium hydroxide done
clear
C)
Phenol, carbon tetrachloride and NaOH done
clear
D)
None of these done
clear
View Solution play_arrow
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question_answer18)
If formaldehyde and potassium hydroxide are heated, then we get [CPMT 1989, 90; KCET 2000]
A)
Acetylene done
clear
B)
Methane done
clear
C)
Methyl alcohol done
clear
D)
Ethyl formate done
clear
View Solution play_arrow
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question_answer19)
An organic compound dissolved in dry benzene evolved hydrogen on treatment with sodium. It is [NCERT 1981; SCRA 1990]
A)
A ketone done
clear
B)
An aldehyde done
clear
C)
A tertiary amine done
clear
D)
An alcohol done
clear
View Solution play_arrow
-
question_answer20)
\[A\underset{\text{dil}\text{. }{{H}_{2}}S{{O}_{4}}}{\mathop{\xrightarrow{{{K}_{2}}C{{r}_{2}}{{O}_{7}}}}}\,B\underset{{{H}_{2}}O}{\mathop{\xrightarrow{C{{H}_{3}}MgI}}}\,C{{H}_{3}}-\underset{OH\ \ \ \ \ \ }{\overset{C{{H}_{3}}\ \ \ \ }{\mathop{\underset{|}{\overset{|}{\mathop{C}}}\,-C{{H}_{3}}}}}\,\]. The reactant A is [MH CET 2002, 03; AFMC 2004; MP PMT/PET 1988; EAMCET 1989; CPMT 1988; MP PET 2000]
A)
\[C{{H}_{3}}CHOHC{{H}_{3}}\] done
clear
B)
\[C{{H}_{3}}COC{{H}_{3}}\] done
clear
C)
\[{{C}_{2}}{{H}_{5}}OH\] done
clear
D)
\[C{{H}_{3}}COOH\] done
clear
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-
question_answer21)
The reaction, water gas \[(CO+{{H}_{2}})+{{H}_{2}}\,\,673K,\,300\] atmosphere in presence of the catalyst \[C{{r}_{2}}{{O}_{3}}/ZnO\] is used for the manufacture of [MP PMT 1989]
A)
HCHO done
clear
B)
HCOOH done
clear
C)
\[C{{H}_{3}}OH\] done
clear
D)
\[C{{H}_{3}}COOH\] done
clear
View Solution play_arrow
-
question_answer22)
\[C{{H}_{2}}=C{{H}_{2}}+{{B}_{2}}{{H}_{6}}\]\[\underset{{{H}_{2}}S{{O}_{4}}}{\mathop{\xrightarrow{NaOH}}}\,\ \text{Product}\text{.}\] Product in above reaction is [RPMT 2003]
A)
\[C{{H}_{3}}C{{H}_{2}}CHO\] done
clear
B)
\[C{{H}_{3}}C{{H}_{2}}OH\] done
clear
C)
\[C{{H}_{3}}CHO\] done
clear
D)
None of these done
clear
View Solution play_arrow
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question_answer23)
Phenolphthalein is obtained by heating phthalic anhydride with conc. \[{{H}_{2}}S{{O}_{4}}\] and [BHU 1996]
A)
Benzyl alcohol done
clear
B)
Benzene done
clear
C)
Phenol done
clear
D)
Benzoic acid done
clear
View Solution play_arrow
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question_answer24)
Maltose on hydrolysis gives [BHU 1996; CPMT 2001]
A)
Mannose + glucose done
clear
B)
Galactose + glucose done
clear
C)
Glucose done
clear
D)
Mannose + fructose done
clear
View Solution play_arrow
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question_answer25)
Absolute alcohol can be obtained from rectified spirit [KCET 1985]
A)
By removing the water in it using concentrated sulphuric acid done
clear
B)
By removing the water using phosphorus pentoxide done
clear
C)
By distilling with the appropriate amount of benzene done
clear
D)
By distilling over plenty of quick lime done
clear
View Solution play_arrow
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question_answer26)
Grignard reagent reacts with compounds containing which of the following groups [MNR 1987]
A)
\[>C=O\] done
clear
B)
\[-C\equiv N\] done
clear
C)
\[>C=S\] done
clear
D)
All of these done
clear
View Solution play_arrow
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question_answer27)
Oil \[+NaO{{H}_{(aq)}}\xrightarrow{\Delta }\]Glycerol + Soap Above reaction is called [UPSEAT 2001]
A)
Saponification done
clear
B)
Esterification done
clear
C)
Hydrogenation done
clear
D)
None of these done
clear
View Solution play_arrow
-
question_answer28)
Acetone on treatment with \[C{{H}_{3}}-Mg-I\] and on further hydrolysis gives [UPSEAT 2000]
A)
Isopropyl alcohol done
clear
B)
Primary alcohol done
clear
C)
Acetic acid done
clear
D)
2-methyl 2-propanol done
clear
View Solution play_arrow
-
question_answer29)
In the following reaction 'A' is \[\begin{align} & {{C}_{2}}{{H}_{5}}MgBr+{{H}_{2}}C-C{{H}_{2}}\xrightarrow{{{H}_{2}}O}A \\ & \,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\overset{\backslash /}{\mathop{O}}\, \\ \end{align}\] [MP PET 1994; CBSE PMT 1998]
A)
\[{{C}_{2}}{{H}_{5}}C{{H}_{2}}CHO\] done
clear
B)
\[{{C}_{2}}{{H}_{5}}C{{H}_{2}}C{{H}_{2}}OH\] done
clear
C)
\[{{C}_{2}}{{H}_{5}}C{{H}_{2}}OH\] done
clear
D)
\[{{C}_{2}}{{H}_{5}}CHO\] done
clear
View Solution play_arrow
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question_answer30)
Sodium benzene sulphonate reacts with NaOH and then on acidic hydrolysis, it gives [Roorkee 1995; KCET 1998]
A)
Phenol done
clear
B)
Benzoic acid done
clear
C)
Benzene done
clear
D)
Disodium benzaldehyde done
clear
View Solution play_arrow
-
question_answer31)
Phenol is obtained by heating aqueous solution of [MP PMT 1995]
A)
Aniline done
clear
B)
Benzene diazonium chloride done
clear
C)
Benzoic acid done
clear
D)
None of these done
clear
View Solution play_arrow
-
question_answer32)
\[{{C}_{2}}{{H}_{5}}MgI\] reacts with HCHO to form last product [MP PMT 1991]
A)
\[C{{H}_{3}}CHO\] done
clear
B)
\[{{C}_{3}}{{H}_{7}}OH\] done
clear
C)
\[C{{H}_{3}}COC{{H}_{3}}\] done
clear
D)
\[C{{H}_{3}}COOC{{H}_{3}}\] done
clear
View Solution play_arrow
-
question_answer33)
Which one is not synthesized by Grignard reagent [MP PET 1991]
A)
Primary alcohol done
clear
B)
Secondary alcohol done
clear
C)
A ketone done
clear
D)
An ester done
clear
View Solution play_arrow
-
question_answer34)
Reaction of aqueous sodium hydroxide on (i) ethyl bromide and (ii) chlorobenzene gives
A)
(i) Ethene and (ii) o-chlorophenol done
clear
B)
(i) Ethyl alcohol and (ii) o-chlorophenol done
clear
C)
(i) Ethyl alcohol and (ii) phenol done
clear
D)
(i) Ethyl alcohol an d(ii) no reaction done
clear
View Solution play_arrow
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question_answer35)
RMgBr on reaction with an excess of oxygen followed by hydrolysis gives [Roorkee Qualifying 1998]
A)
RH done
clear
B)
ROOR done
clear
C)
ROOH done
clear
D)
ROH done
clear
View Solution play_arrow
-
question_answer36)
The reaction between an ester and excess of Grignard reagent shall finally result in a [UPSEAT 2000]
A)
Primary alcohol done
clear
B)
Secondary alcohol done
clear
C)
Tertiary alcohol done
clear
D)
Ketone done
clear
View Solution play_arrow
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question_answer37)
The compound that will react most readily with NaOH to form methanol is [IIT-JEE (Screening) 2001]
A)
\[{{(C{{H}_{3}})}_{4}}{{N}^{+}}{{I}^{-}}\] done
clear
B)
\[C{{H}_{3}}OC{{H}_{3}}\] done
clear
C)
\[{{(C{{H}_{3}})}_{3}}{{S}^{+}}{{I}^{-}}\] done
clear
D)
\[{{(C{{H}_{3}})}_{3}}Cl\] done
clear
View Solution play_arrow
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question_answer38)
When 2-ethylanthraquinol dissolved in a mixture of benzene and cyclohexanol is oxidised, the product is [JIPMER 1999]
A)
Ethanol done
clear
B)
Hydrogen peroxide done
clear
C)
Anthracene done
clear
D)
None of these done
clear
View Solution play_arrow
-
question_answer39)
Which gas is eliminated in fermentation [RPMT 1997]
A)
\[{{O}_{2}}\] done
clear
B)
\[C{{O}_{2}}\] done
clear
C)
\[{{N}_{2}}\] done
clear
D)
\[{{H}_{2}}\] done
clear
View Solution play_arrow
-
question_answer40)
Action of nitrous acid with ethylamine produces [BHU 2000]
A)
Ethane done
clear
B)
Ammonia done
clear
C)
Ethyl alcohol done
clear
D)
Nitroethane done
clear
View Solution play_arrow
-
question_answer41)
The product of reduction of benzaldehyde is
A)
Benzoic acid done
clear
B)
Benzyl alcohol done
clear
C)
Benzene done
clear
D)
Catechol done
clear
View Solution play_arrow
-
question_answer42)
Commercially methanol is prepared by [IIT 1984; MP PMT 1990; KCET 1992]
A)
Reduction of CO in presence of \[ZnO.C{{r}_{2}}{{O}_{3}}\] done
clear
B)
Methane reacts with water vapours at \[{{900}^{o}}C\] in presence of Ni catalyst done
clear
C)
Reduction of HCHO by \[LiAl{{H}_{4}}\] done
clear
D)
Reduction of HCHO by aqueous NaOH done
clear
View Solution play_arrow
-
question_answer43)
Action of water in the presence of sulphuric acid with the following alkenes (i) \[C{{H}_{3}}-CH=C<\begin{matrix} C{{H}_{3}} \\ C{{H}_{3}} \\ \end{matrix}\] and (ii) \[C{{H}_{3}}-CH=C{{H}_{2}}\] gives
A)
\[C{{H}_{3}}-C{{H}_{2}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,\ \ }}\,<\begin{matrix} C{{H}_{3}} \\ C{{H}_{3}} \\ \end{matrix}\] and (ii) \[C{{H}_{3}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,H}}\,-C{{H}_{3}}\] done
clear
B)
(i) \[C{{H}_{3}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,H}}\,=CH<\begin{matrix} C{{H}_{3}} \\ C{{H}_{3}} \\ \end{matrix}\] and(ii) \[C{{H}_{3}}-C{{H}_{2}}-C{{H}_{2}}OH\] done
clear
C)
(i) \[C{{H}_{3}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,H}}\,-CH<\begin{matrix} C{{H}_{3}} \\ C{{H}_{3}} \\ \end{matrix}\] and (ii) \[C{{H}_{3}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,H}}\,-C{{H}_{3}}\] done
clear
D)
(i) \[C{{H}_{3}}-C{{H}_{2}}-\underset{OH}{\mathop{\underset{|}{\mathop{C}}\,\ \ }}\,<\begin{matrix} C{{H}_{3}} \\ C{{H}_{3}} \\ \end{matrix}\] and(ii) \[C{{H}_{3}}-C{{H}_{2}}-C{{H}_{2}}OH\] done
clear
View Solution play_arrow
-
question_answer44)
From Williamson?s synthesis preparation of which of following is possible
A)
Only symmetrical ethers done
clear
B)
Only symmetrical ethers done
clear
C)
Both types done
clear
D)
None of these done
clear
View Solution play_arrow
-
question_answer45)
In the reaction \[Ar-OH+Rx\xrightarrow{\text{alkali}}A,\] A is [MP PET 1994]
A)
An aldehyde done
clear
B)
An aryl chloride done
clear
C)
An ether done
clear
D)
A ketone done
clear
View Solution play_arrow
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question_answer46)
Williamson's synthesis is used to prepare [DPMT 1976, 81, 82, 83, 84; CPMT 1976, 82]
A)
Acetone done
clear
B)
Diethyl ether done
clear
C)
P.V.C. done
clear
D)
Bakelite done
clear
View Solution play_arrow
-
question_answer47)
When an alkyl halide is allowed to react with a sodium alkoxide the product most likely is [MP PMT 1996; EAMCET 1998]
A)
An aldehyde done
clear
B)
A ketone done
clear
C)
An ether done
clear
D)
A carboxylic acid done
clear
View Solution play_arrow
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question_answer48)
In Williamson's synthesis, ethoxyethane is prepared by [MP PMT 1995; BHU 2005]
A)
Passing ethanol over heated alumina done
clear
B)
Sodium ethoxide with ethyl bromide done
clear
C)
Ethyl alcohol with sulphuric acid done
clear
D)
Ethyl iodide and dry silver oxide done
clear
View Solution play_arrow
-
question_answer49)
Formation of diethyl ether from ethanol is based on a [BVP 2003]
A)
Dehydration reaction done
clear
B)
Dehydrogenation reaction done
clear
C)
Hydrogenation reaction done
clear
D)
Heterolytic fission reaction done
clear
View Solution play_arrow
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question_answer50)
The compound formed when ethyl bromide is heated with dry silver oxide is [MP PET/PMT 1988]
A)
Dimethyl ether done
clear
B)
Diethyl ether done
clear
C)
Methyl alcohol done
clear
D)
Ethyl alcohol done
clear
View Solution play_arrow
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question_answer51)
The reagent used for the preparation of higher ether from halogenated ethers is [Tamil Nadu CET 2001]
A)
conc. \[{{H}_{2}}S{{O}_{4}}\] done
clear
B)
Sodium alkoxide done
clear
C)
Dry silver oxide done
clear
D)
Grignard reagent done
clear
View Solution play_arrow
-
question_answer52)
Acetyl bromide reacts with excess of \[C{{H}_{3}}MgI\] followed by treatment with a saturated solution of \[N{{H}_{4}}Cl\] gives [AIEEE 2004]
A)
2-methyl-2-propanol done
clear
B)
Acetamide done
clear
C)
Acetone done
clear
D)
Acetyl iodide done
clear
View Solution play_arrow
-
question_answer53)
What is obtained when chlorine is passed in boiling toluene and product is hydrolysed [DCE 2004]
A)
o-Cresol done
clear
B)
p-Cresol done
clear
C)
2, 4-Dihydroxytoluene done
clear
D)
Benzyl alcohol done
clear
View Solution play_arrow
-
question_answer54)
Which of the following is formed when benzaldehyde reacts with sodium hydroxide [Pb. CET 2002]
A)
Benzyl alcohol done
clear
B)
Benzoic acid done
clear
C)
Glucose done
clear
D)
Acetic acid done
clear
View Solution play_arrow
-
question_answer55)
When ethanal reacts with \[C{{H}_{3}}MgBr\] and \[{{C}_{2}}{{H}_{5}}OH\]/dry HCl the product formed are [DCE 2003]
A)
Ethyl alcohol and 2-propanol done
clear
B)
Ethane and hemi-acetal done
clear
C)
2-propanol and acetal done
clear
D)
Propane and methyl acetate done
clear
View Solution play_arrow
-
question_answer56)
Which of the following is industrially prepared by passing ethylene into hypochlorous acid [BHU 2004]
A)
Ethylene glycol done
clear
B)
Ethylene oxide done
clear
C)
Ethylene dinitrate done
clear
D)
Ethane done
clear
View Solution play_arrow
-
question_answer57)
In which case methyl-t-butyl ether is formed [Orissa JEE 2004]
A)
\[{{({{C}_{2}}{{H}_{5}})}_{3}}CONa+C{{H}_{3}}Cl\] done
clear
B)
\[{{(C{{H}_{3}})}_{3}}CONa+C{{H}_{3}}Cl\] done
clear
C)
\[{{(C{{H}_{3}})}_{3}}CONa+{{C}_{2}}{{H}_{5}}Cl\] done
clear
D)
\[{{(C{{H}_{3}})}_{3}}CONa+C{{H}_{3}}Cl\] done
clear
View Solution play_arrow
-
question_answer58)
Which of the following combinations can be used to synthesize ethanol [KCET 2004]
A)
\[C{{H}_{3}}MgI\] and \[C{{H}_{3}}COC{{H}_{3}}\] done
clear
B)
\[C{{H}_{3}}MgI\] and \[{{C}_{2}}{{H}_{5}}OH\] done
clear
C)
\[C{{H}_{3}}MgI\] and \[C{{H}_{3}}COO{{C}_{2}}{{H}_{5}}\] done
clear
D)
\[C{{H}_{3}}MgI\] and \[HCOO{{C}_{2}}{{H}_{5}}\] done
clear
View Solution play_arrow
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question_answer59)
\[{{C}_{6}}{{H}_{5}}-CH=CHCHO\xrightarrow{X}{{C}_{6}}{{H}_{5}}CH=CHC{{H}_{2}}OH\]. In the above sequence X can be [DCE 2004]
A)
\[{{H}_{2}}/Ni\] done
clear
B)
\[NaB{{H}_{4}}\] done
clear
C)
\[{{K}_{2}}C{{r}_{2}}{{O}_{7}}/{{H}^{+}}\] done
clear
D)
Both A and B done
clear
View Solution play_arrow
-
question_answer60)
Alkenes convert into alcohols by [MP PET 1991]
A)
Hydrolysis by dil. \[{{H}_{2}}S{{O}_{4}}\] done
clear
B)
Hydration of alkene by alkaline \[KMn{{O}_{4}}\] done
clear
C)
Hydrolysis by water vapours and conc. \[{{H}_{2}}S{{O}_{4}}\] done
clear
D)
Hydration of alkene by aqueous KOH done
clear
View Solution play_arrow
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question_answer61)
Acetic acid and \[C{{H}_{3}}OH\] are obtained on large scale by destructive distillation of
A)
Wood done
clear
B)
Coal done
clear
C)
Turpentine done
clear
D)
Crude oil done
clear
View Solution play_arrow
-
question_answer62)
Which is formed when benzalamine react with nitrous acid [KCET (Med.) 2001]
A)
\[{{C}_{6}}{{H}_{5}}OH\] done
clear
B)
\[{{C}_{6}}{{H}_{5}}ON\] done
clear
C)
\[{{C}_{2}}{{H}_{5}}{{N}_{2}}OH\] done
clear
D)
\[{{C}_{6}}{{H}_{5}}C{{H}_{2}}OH\] done
clear
View Solution play_arrow
-
question_answer63)
Acid catalyzed hydration of alkenes except ethene leads to the formation of [AIEEE 2005]
A)
Primary alcohol done
clear
B)
Secondary or tertiary alcohol done
clear
C)
Mixture of primary and secondary alcohols done
clear
D)
Mixture of secondary and tertiary alcohols done
clear
View Solution play_arrow
-
question_answer64)
Methylphenyl ether can be obtained by reacting [J & K 2005]
A)
Phenolate ions and methyl iodide done
clear
B)
Methoxide ions and bromobenzene done
clear
C)
Methanol and phenol done
clear
D)
Bromo benzene and methyl bromide done
clear
View Solution play_arrow