Sr. # | Questions | Answers Choice |
---|---|---|
1 | To prepare ethane by Wurtz synthesis the suitable alkyl halide is |
Ethyl iodide any alkyl iodide Ethyl chloride Methyl bromide |
2 | Reaction of ethyl bromide with ammonia | <div>Completes in a single step</div><div><br></div> Completes in two steps Continues till N is left with no lone pair is reversible |
3 | In beta elimination reaction | carbon number changes unsaturated compound is formed hybridization. ofC remains same pi bonds are decreased |
4 | Which is an intermediate in SN1 reaction | Ethoxide ion Carbocation alkyl halide alkene |
5 | The reagent for alkaline hydrolysis of ethyl bromide to form ethyl alcohol is | water at room T Alcoholic KOH+heat Ethanol + heat dil. NaOH+ heat |
6 | Which pair gives same dehydrohalogenation product | <div>I-Chlorobutane, 2-Chlorobutane</div><div><br></div> I-Chloropropane, 2-Chloropropane I-Bromopentane. 3-Bromopentane iso-butvl chloride. 2°- butyl chloride |
7 | In an elimination reaction a more substituted alkene is formed due to the stability associated with | Free radical transition state Activated complex Carbocation |
8 | Dehydrohalogenation of secondary butyI bromide will give | Propene 1-Butene Butene 2-Butene |
9 | Which of the following reactants will be required to form ethene from ethyl chloride | <sub>Alcoholic KOH</sub> Alkaline KMnO4 Aqucous KOH Aqucous NaOH |
10 | Which one among the following is not a good leaving group | HSO4- CI- OH- Br- |
11 | In nucleophilie substitution bimolecular reaction the order of reaction with respect to substrate | 2 order 3 order 1st order Zero order |
12 | Which compound is obtained hy the elimination reaction on bromoethane? | Butene Ethene Propene Propane |
13 | When 2-bromobutane reacts with alcoholic KOH, the reaction is called | Chlorination Halogenation Dehydrohalogenation Hydrogenation |
14 | Which of the following alkyl halides undergoes SN1 reaction fastest | Methyl chloride Isobutyl chlorido Ethy l chloride Tertiary butyl chloride |
15 | A mixture of 1-chloropropane and 2-chloro-propane when treated with alcoholic KOH, gives | Prop-2-ene Isopropy lene Propene A mixture of prop-l-ene |
16 | In elimination reaction i.e, in the formation of alkene, the reactivity of alkyl halide is in the order: | CI>Br>I I>Br>Cl Br>CI>I I>CI> Br |
17 | The species which are produced by heterolytic bond breaking and can act as electron pair donor | Free radicals Cations Nucleophiles electrophile |
18 | Among the following, which one is nucleophile | H+ Ca2+ OH- Na+ |
19 | Which is an intermediate in Svl | Ethoxide ion Alkene Alkyl halide Carbocation |
20 | Which one of the following is NOT a nucleophile | NH2+ BF3 H2O CH3- |
21 | The order of reactivitv of alksI halides towards nucleophile is | RI>RBr RF>RCI RF>RCI>RBr>RI RI>RBr> RCI>RE RF>RBr>RCI>RI |
22 | The alkaline hydrolysis of bromoethane shown below gives alcohol as the product: H3C-CH2-Br-------H3C-CH2-OH The reagent and the condition used in this reaction may be: |
H20 at room temperature KOH in alcohol Ethanol. heat Dilute NaOH(aq) warm |
23 | When purely alcoholic solution of sodium/potassiumhydroxide and halogenoalkanes are reacted an alkene is formed, what is the mechanism of reaction? | Elimination Debromination Dehydration Reduction |
24 | Correct order for the reactivity ofalkyl halide in S, reactions | R-I>R-F>R-CI R-F>R-CI>R-I R-I>R-CI>R-F R-CI>R-I>R-F |
25 | Correct statement about Nucleophilic substitution bimolecular is | Transition state is formed Inversion take place It is two step reacticn Both a &c |
26 | The reaction C2H5CI + aqueous KOH---------C2H5OH+ KCI is | Electrophilic addition Nucleophilic addition Electrophilic substitution Nucleophilic substitution |
27 | An alkyl halide reacts with NH3 to give | Amide Cyanide Amine Aniline |
28 | Out of monochloro, monobromo and mongiodo derivatives of ethane, the mos reactive compound towards nucleophilic substitution will be | C2H5Br C2H5Cl C2H5I All are equally reactive |
29 | Elimination unimolecular reactions involve | Second order kinetics First order kinetics Third order kinetics Zero order kinetics |
30 | Which of the following is primary alkyl halide | IsopropyI halide Sec-butyl halide Tert-buryi halide Neo-pentyl halide |
31 | Which isomer of C4H9Br will produce 2-methyl propane-2-ol on treatment with aqueous KOH | n-butyI bromide Sec-butyI bromide Isobutyl halide Tertiary butyl chloride |
32 | Which one of the following is not associated with SN2 mechanism | 100 % inversion of configuration Tertiar alkyI halides 2nd order kinetics Change of hy bridization from sp³ to sp² in transition state |
33 | Which of the following factors does not affect the SN1 rate is | Nucleophilicity of the attacking nucleophile Stability of the carbonium ion Solvent system The nature of leaving group |
34 | In the transition state of S2 mechanism reaction with alkyl halides, which of the following orbital hybridization is involved | sp³ sp sp² dsp³ |
35 | Which of the following decides the reactivity of alkyl halides? | C-C bond strength C-H bond strength C-X bond strength Electronegativity difference |
36 | Chloroform (CHCl3) is? | Primary alkyl halide Secondary alkyl halide Tertiary alkyl halide a liquid |
37 | Which is a good nucleophile as well as a good leaving group? | F- Cl- Br- I- |
38 | An amine is produced in the following reaction C2H5l+2NH3-------C2H5NH2 +NH4l. What is mechanism? |
Electrophilic addition Electrophilic substitution Nucleophilic addition Nucleophilic substitution |
39 | The Sl mechanism for the hydrolysis of an alkyl halide to an alcohol involves the formation of | Carbocation Carbanion Pentavalent carbon in the transition state Free radical |
40 | SN2-reactions can be usually observed in | Primary alkylı halide secondary alkyl halide Tertiary alkyl halide Both A. and B |
41 | Alkyl halides are considered to be very reactive compounds towards nucleophiles, because | The have an electrophilic carbon They have an electrophilic carbon and a bad leaving group They have an electrophilic carbon and a good laving group They have a nucleophilic carbon and a good leaving group |
42 | The rate of E1 reaction depends upon | The concentration of substrate The concentration of substrate as well as nucleophile The concentration Nucleophilic Nature of Catalyst |
43 | For which mechanisms, the first step involved is the same | E1 and E2 E2 and SN2 E2 and E1 E1 and SN1 |
44 | The average bond energy of C-Br is | 228 kJmol-1 250 kJmol-1 200 kJmol-1 290 kJmol-1 |
45 | The carbon atom of an alkyl group attached with halogen atom is called | Electrophile Free redical Nucleophile Nucleophilic centre |
46 | Hydration of ethene is an example of | Electrophilic addition Electrophilic substitution Nucleophilic addition Nucleophilic substitution |
47 | Ethyl and methyl groups are equidistant in a chain, the preference is given to? | Ethyl methyl both ethyl and methyl methyl mostly |
48 | Tertiary alcohols are the easiest to dehydrate because | They form stable carbocation They have less hydrogen They have bigger size They are polar |
49 | The reaction of alkyl halide in the presence of alcoholic KOH is | Substitution Addition Acid-base Elimination |
50 | Which group activates the benzene ring | -COOH -COR -CHO -OH |
51 | Benzene reacts with Ethyl chloride in presence of AICls to give | Benzalchloride Benzyl chloride Ethyl benzene Benzotrichloride |
52 | Ethene can give all of the following reactions except | Addition Free radical substitution Hydrohalogenation Hydration |
53 | Active sulphonating agent during sulphonation of benzene is | SO2 SO3 SO3H SO3+ |
54 | Glyoxal molecule has? | two carbonyl groups One aldehydic and one carbonyl group Two aldehydic groups Two carboxyl group |
55 | Ethane when completely halogenated in excess of chiorine can form | Hexachloroethane Dichloroethane Pentachloroethane 1.1.2.2-terachloroethane |
56 | The origin ofacidic nature of alkyne is? | small size of C Small size of H polarity of triple bond sp hybridization |
57 | A compound that has a nucleophilic carbon? | C2H2 C2H4 C3H8 C6H6 |
58 | The addition of HCI to ethene gives? | Chloroethane 1,2-dichloroethane 1.1-dichloroethane 2-chloroethane |
59 | The reaction that generates an ionic bond is | Halogenation of ethene polymerization of ethene Hydrogenation of ethyne Reaction of ethyne withs sodamide |
60 | Acetylide can give back ethyne upon treatment with | water strong base dil. Acid weak base |