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
1,301
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,302
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
1,303
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,304
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
1,305
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
1,306
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
1,307
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
1,308
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,309
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,310
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,311
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,312
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
1,313
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
1,314
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,315
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,316
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
1,317
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
1,318
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,319
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
1,320
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
1,321
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,322
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,323
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
1,324
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
1,325
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
1,326
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
1,327
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
1,328
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
1,329
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
1,330
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,331
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
1,332
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
1,333
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,334
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,335
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
1,336
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
1,337
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
1,338
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,339
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
1,340
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
1,341
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
1,342
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
1,343
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,344
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,345
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
1,346
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,347
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,348
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
1,349
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
1,350
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
1,351
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,352
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
1,353
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
1,354
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
1,355
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
1,356
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
1,357
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
1,358
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
1,359
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,360
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
1,361
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
1,362
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
1,363
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
1,364
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,365
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
1,366
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
1,367
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
1,368
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
1,369
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,370
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,371
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
1,372
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
1,373
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
1,374
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
1,375
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
1,376
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,377
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,378
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
1,379
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
1,380
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
1,381
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
1,382
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,383
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
1,384
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
1,385
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
1,386
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
1,387
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
1,388
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
1,389
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,390
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,391
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
1,392
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
1,393
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
1,394
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
1,395
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
1,396
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
1,397
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,398
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
1,399
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
1,400
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard