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
8,601
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
8,602
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,603
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,604
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
8,605
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
8,606
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
8,607
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
8,608
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,609
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
8,610
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
8,611
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
8,612
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,613
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,614
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
8,615
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,616
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
8,617
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,618
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
8,619
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
8,620
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
8,621
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
8,622
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,623
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
8,624
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,625
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
8,626
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
8,627
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
8,628
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,629
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
8,630
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
8,631
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
8,632
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
8,633
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
8,634
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
8,635
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
8,636
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
8,637
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
8,638
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,639
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,640
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
8,641
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,642
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
8,643
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
8,644
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
8,645
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
8,646
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
8,647
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,648
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
8,649
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
8,650
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
8,651
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
8,652
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
8,653
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,654
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
8,655
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
8,656
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
8,657
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
8,658
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
8,659
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
8,660
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
8,661
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
8,662
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
8,663
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
8,664
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
8,665
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,666
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,667
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
8,668
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
8,669
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,670
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
8,671
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
8,672
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
8,673
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,674
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
8,675
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,676
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
8,677
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
8,678
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
8,679
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,680
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
8,681
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
8,682
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
8,683
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
8,684
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
8,685
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
8,686
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
8,687
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
8,688
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
8,689
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
8,690
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,691
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
8,692
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
8,693
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
8,694
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
8,695
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
8,696
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
8,697
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
8,698
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
8,699
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
8,700
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