Row_ID
int64
1
30.2M
Topic
stringclasses
3 values
Subtopic
stringclasses
4 values
Question
stringclasses
13 values
Answer_1
stringclasses
11 values
Explanation_1
stringclasses
12 values
Answer_2
stringclasses
11 values
Explanation_2
stringclasses
11 values
Answer_3
stringclasses
0 values
Explanation_3
stringclasses
0 values
Difficulty
stringclasses
2 values
9,301
Organic Chemistry
Alkenes
HCl+2-methylpropene product?
2-chloro-2-methylpropane
HCl adds; yields 2-chloro-2-methylpropane.
tert-butyl chloride
Same: tert-butyl chloride.
null
null
Hard
9,302
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,303
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,304
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,305
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,306
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,307
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,308
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,309
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,310
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,311
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,312
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,313
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,314
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,315
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,316
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,317
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,318
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,319
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,320
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,321
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,322
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,323
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,324
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,325
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,326
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,327
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,328
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,329
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,330
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,331
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,332
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,333
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,334
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,335
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,336
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,337
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,338
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,339
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,340
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,341
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,342
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,343
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,344
Organic Chemistry
Alkenes
HCl+2-methylpropene product?
2-chloro-2-methylpropane
HCl adds; yields 2-chloro-2-methylpropane.
tert-butyl chloride
Same: tert-butyl chloride.
null
null
Hard
9,345
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,346
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,347
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,348
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,349
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,350
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,351
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,352
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,353
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,354
Organic Chemistry
Alkenes
HCl+2-methylpropene product?
2-chloro-2-methylpropane
HCl adds; yields 2-chloro-2-methylpropane.
tert-butyl chloride
Same: tert-butyl chloride.
null
null
Hard
9,355
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,356
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
9,357
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,358
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
9,359
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,360
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,361
Organic Chemistry
Alkenes
HBr+1-methylcyclohexene product?
1-bromo-1-methylcyclohexane
HBr adds; yields 1-bromo-1-methylcyclohexane.
1-methyl-1-bromocyclohexane
Same: 1-methyl-1-bromocyclohexane.
null
null
Hard
9,362
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,363
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,364
Organic Chemistry
Alkenes
HBr+1-methylcyclohexene product?
1-bromo-1-methylcyclohexane
HBr adds; yields 1-bromo-1-methylcyclohexane.
1-methyl-1-bromocyclohexane
Same: 1-methyl-1-bromocyclohexane.
null
null
Hard
9,365
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,366
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,367
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,368
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,369
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,370
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,371
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,372
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,373
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,374
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,375
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,376
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,377
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,378
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,379
Organic Chemistry
Alkenes
HBr+1-methylcyclohexene product?
1-bromo-1-methylcyclohexane
HBr adds; yields 1-bromo-1-methylcyclohexane.
1-methyl-1-bromocyclohexane
Same: 1-methyl-1-bromocyclohexane.
null
null
Hard
9,380
Organic Chemistry
Alkenes
HBr+1-methylcyclohexene product?
1-bromo-1-methylcyclohexane
HBr adds; yields 1-bromo-1-methylcyclohexane.
1-methyl-1-bromocyclohexane
Same: 1-methyl-1-bromocyclohexane.
null
null
Hard
9,381
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,382
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,383
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,384
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,385
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
9,386
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,387
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,388
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,389
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
9,390
Physical Chemistry
Kinetics
t1/2,k=0.1s^-1?
6.9s
t1/2=0.693/0.1=6.9s.
~7s
t1/2β‰ˆ0.7/0.1=7s.
null
null
Hard
9,391
Inorganic Chemistry
Oxidation States
Co ox.state in [Co(NH3)6]3+?
+3
[Co(NH3)6]3+: Co=+3.
Co(III)
+3=III.
null
null
Expert
9,392
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,393
Physical Chemistry
Kinetics
t1/2,k=0.05s^-1?
13.9s
t1/2=0.693/0.05=13.9s.
~14s
t1/2β‰ˆ0.7/0.05=14s.
null
null
Hard
9,394
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,395
Physical Chemistry
Kinetics
t1/2,k=0.02s^-1?
34.6s
t1/2=0.693/0.02=34.6s.
~35s
t1/2β‰ˆ0.7/0.02=35s.
null
null
Hard
9,396
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
null
null
Expert
9,397
Organic Chemistry
Alkenes
HBr+1-methylcyclohexene product?
1-bromo-1-methylcyclohexane
HBr adds; yields 1-bromo-1-methylcyclohexane.
1-methyl-1-bromocyclohexane
Same: 1-methyl-1-bromocyclohexane.
null
null
Hard
9,398
Physical Chemistry
Kinetics
t1/2,k=0.01s^-1?
69.3s
t1/2=0.693/0.01=69.3s.
~70s
t1/2β‰ˆ0.7/0.01=70s.
null
null
Hard
9,399
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
9,400
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard