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
4,401
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
4,402
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
4,403
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
4,404
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
4,405
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
4,406
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,407
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
4,408
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,409
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
4,410
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
4,411
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
4,412
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
4,413
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,414
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
4,415
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
4,416
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
4,417
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,418
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
4,419
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
4,420
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
4,421
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,422
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,423
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
4,424
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
4,425
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
4,426
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,427
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,428
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
4,429
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
4,430
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
4,431
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
4,432
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
4,433
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
4,434
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,435
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
4,436
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
4,437
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,438
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
4,439
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
4,440
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
4,441
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
4,442
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
4,443
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,444
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,445
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,446
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
4,447
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,448
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
4,449
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,450
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
4,451
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
4,452
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
4,453
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,454
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
4,455
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,456
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
4,457
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
4,458
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
4,459
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,460
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
4,461
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
4,462
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
4,463
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,464
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,465
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
4,466
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
4,467
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
4,468
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
4,469
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
4,470
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
4,471
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
4,472
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
4,473
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
4,474
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,475
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
4,476
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
4,477
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
4,478
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
4,479
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
4,480
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,481
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
4,482
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
4,483
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
4,484
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
4,485
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
4,486
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
4,487
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
4,488
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
4,489
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
4,490
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,491
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
4,492
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
4,493
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
4,494
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
4,495
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
4,496
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
4,497
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
4,498
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
4,499
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
4,500
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard