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
1,201
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
1,202
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
1,203
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
1,204
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
1,205
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
1,206
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
1,207
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,208
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
1,209
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
1,210
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
1,211
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,212
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
1,213
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
1,214
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
1,215
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
1,216
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
1,217
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
1,218
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
1,219
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
1,220
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
1,221
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,222
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
1,223
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
1,224
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
1,225
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
1,226
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
1,227
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
1,228
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
1,229
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
1,230
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,231
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
1,232
Organic Chemistry
Alkenes
HCl+1-methylcyclohexene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,233
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
1,234
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,235
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,236
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
1,237
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
1,238
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,239
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
1,240
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
1,241
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
1,242
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,243
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
1,244
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
1,245
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,246
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
1,247
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
1,248
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
1,249
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
1,250
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
1,251
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
1,252
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
1,253
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,254
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
1,255
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,256
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
1,257
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
1,258
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
1,259
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
1,260
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,261
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
1,262
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
1,263
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
1,264
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,265
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,266
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
1,267
Organic Chemistry
Alkenes
HBr+2-methylpropene product?
unknown
HBr adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,268
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
1,269
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
1,270
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,271
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
1,272
Organic Chemistry
Alkenes
HCl+1-butene product?
unknown
HCl adds; yields unknown.
unknown
Same: unknown.
null
null
Hard
1,273
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
1,274
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
1,275
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
1,276
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,277
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
1,278
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
1,279
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
1,280
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
1,281
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
1,282
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
1,283
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
1,284
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
1,285
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
1,286
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
1,287
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
1,288
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
1,289
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,290
Organic Chemistry
Alkenes
HBr+1-butene product?
2-bromobutane
HBr adds; yields 2-bromobutane.
sec-butyl bromide
Same: sec-butyl bromide.
null
null
Hard
1,291
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
null
null
Hard
1,292
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
1,293
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
1,294
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
1,295
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
1,296
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
1,297
Inorganic Chemistry
Oxidation States
Fe ox.state in [Fe(CN)6]4-?
+2
[Fe(CN)6]4-: Fe=+2.
Fe(II)
+2=II.
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Expert
1,298
Organic Chemistry
Nomenclature
Name CH3CH(OH)CH2CHO?
3-hydroxybutanal
CH3CH(OH)CH2CHO: 3-hydroxybutanal.
beta-hydroxybutyraldehyde
3-hydroxybutanal=beta-hydroxybutyraldehyde.
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Hard
1,299
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.
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Hard
1,300
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.
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Hard