問題一覧
1
High melting and boiling points
2
3,3,5-trimethylhexane
3
Propyne
4
-one
5
I only (Alcohol)
6
4-ethyl-2,3-dimethyloctane
7
CH3-CH=CH-CH2-CH3
8
C5H10
9
3
10
1
11
A σ bond has cylindrical symmetry about the bonding axis.
12
Two π bonds and two σ bonds.
13
120°, trigonal planar.
14
sp3
15
σ bond
16
A molecule with a plane of symmetry
17
The molecular configuration is chiral.
18
1-Chloropropene
19
Neither a double bond nor a ring is necessary; the necessary feature is chirality (e.g., a stereogenic center or another element of asymmetry).
20
Enantiomers
21
Dehydration
22
Substitution
23
An electron-deficient species that accepts electron pairs
24
CH3− (methyl anion)
25
A nucleophile must always be negatively charged.
26
Propane and Butane
27
CH4 (methane)
28
Neither higher water solubility nor higher melting points (Neither I nor II)
29
CO2 and H2O
30
Free radical substitution
31
Electrophilic addition
32
Hydrogenation
33
1,2-Dichlorobutane (CH2Cl-CHCl-CH2-CH3)
34
Br2, H2O
35
Ozonolysis
36
The electrophile (e.g., H+) adds to the carbon with more hydrogens
37
1,2-Propanediol (propane-1,2-diol)
38
Reactivity with electrophiles
39
Hydroboration–oxidation of alkenes
40
CH≡C–CH2–CH3 (1-butyne)
41
meta
42
Substitution preserves the stability of the aromatic system.
43
Styrene
44
A Lewis acid
45
No reaction (Friedel–Crafts alkylation does not occur on nitrobenzene under normal conditions because the nitro group strongly deactivates the ring)
46
Alkyl halide (a halogenated alkane, e.g., chlorofluorocarbon)
47
Nucleophile (and often a base)
48
A nucleophile
49
SN2
50
tert-Butyl chloride ((CH3)3CCl)
51
2-methylbutane < n-pentane < butanone < butanol
52
Ether
53
Primary alcohols
54
Nucleophilic addition
55
The carboxylate anion is stabilized by resonance.
56
2-methyl-2-propanol (tert-butanol)
57
Butanoic acid (butyric acid)
58
tert-Butyl chloride (2-chloro-2-methylpropane)
59
Nitrile (–C≡N)
60
Amine
61
Testing and calibration laboratories
62
To validate test accuracy using a sample with a known analyte concentration
63
To assess method recovery and matrix effects by adding a known amount of analyte
64
Quality Assurance
65
Quality Control
66
Control chart (e.g., Shewhart or Levey–Jennings chart)
67
Replicate measurements
68
Running replicates
69
RA 9165
70
RA 9514
71
Away from air supply vents and diffusers
72
Position equipment and chemicals at least 6 inches (15 cm) inside the hood, Avoid sudden sash movements
73
Located next to an exterior door that remains open frequently
74
At least 15 minutes
75
Strong alkalis
76
Remain clear of all items at all times and be marked with yellow and black floor tape to remind users to keep it clear
77
Carbon dioxide - because it displaces oxygen without conducting electricity
78
Class B - Foam or dry chemical extinguisher
79
Red body with no band
80
Oxygen, fuel, heat
81
To ensure consistent, safe chemical handling and regulatory compliance
82
Alerts personnel to potential hazards and facilitates emergency response
83
PPE serves as the last line of defense and must be supported by systemic controls
84
Flame-resistant lab coat
85
Neoprene gloves and a chemical-resistant lab coat
86
Cryogenic gloves and a flame-resistant lab coat
87
N95 respirator
88
Face shield with goggles and full-face respirator
89
It supplies filtered air continuously while reducing breathing effort
90
Anti-fog goggles
91
Acute toxicity (fatal or toxic)
92
Physical hazard
93
Biosafety cabinet use, sterilization, and waste segregation
94
Flammable, self-reactive substances, and pyrophorics
95
Risk of long-term health effects like cancer or reproductive toxicity
96
Safety Data Sheet
97
FLAM (Flammable)
98
Dead tree and fish — environmental hazard
99
Corrosive chemical that can cause skin burns and eye damage
100
16
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100問 • 3ヶ月前PT GEN CHEM
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PT GEN CHEM
100問 • 3ヶ月前問題一覧
1
High melting and boiling points
2
3,3,5-trimethylhexane
3
Propyne
4
-one
5
I only (Alcohol)
6
4-ethyl-2,3-dimethyloctane
7
CH3-CH=CH-CH2-CH3
8
C5H10
9
3
10
1
11
A σ bond has cylindrical symmetry about the bonding axis.
12
Two π bonds and two σ bonds.
13
120°, trigonal planar.
14
sp3
15
σ bond
16
A molecule with a plane of symmetry
17
The molecular configuration is chiral.
18
1-Chloropropene
19
Neither a double bond nor a ring is necessary; the necessary feature is chirality (e.g., a stereogenic center or another element of asymmetry).
20
Enantiomers
21
Dehydration
22
Substitution
23
An electron-deficient species that accepts electron pairs
24
CH3− (methyl anion)
25
A nucleophile must always be negatively charged.
26
Propane and Butane
27
CH4 (methane)
28
Neither higher water solubility nor higher melting points (Neither I nor II)
29
CO2 and H2O
30
Free radical substitution
31
Electrophilic addition
32
Hydrogenation
33
1,2-Dichlorobutane (CH2Cl-CHCl-CH2-CH3)
34
Br2, H2O
35
Ozonolysis
36
The electrophile (e.g., H+) adds to the carbon with more hydrogens
37
1,2-Propanediol (propane-1,2-diol)
38
Reactivity with electrophiles
39
Hydroboration–oxidation of alkenes
40
CH≡C–CH2–CH3 (1-butyne)
41
meta
42
Substitution preserves the stability of the aromatic system.
43
Styrene
44
A Lewis acid
45
No reaction (Friedel–Crafts alkylation does not occur on nitrobenzene under normal conditions because the nitro group strongly deactivates the ring)
46
Alkyl halide (a halogenated alkane, e.g., chlorofluorocarbon)
47
Nucleophile (and often a base)
48
A nucleophile
49
SN2
50
tert-Butyl chloride ((CH3)3CCl)
51
2-methylbutane < n-pentane < butanone < butanol
52
Ether
53
Primary alcohols
54
Nucleophilic addition
55
The carboxylate anion is stabilized by resonance.
56
2-methyl-2-propanol (tert-butanol)
57
Butanoic acid (butyric acid)
58
tert-Butyl chloride (2-chloro-2-methylpropane)
59
Nitrile (–C≡N)
60
Amine
61
Testing and calibration laboratories
62
To validate test accuracy using a sample with a known analyte concentration
63
To assess method recovery and matrix effects by adding a known amount of analyte
64
Quality Assurance
65
Quality Control
66
Control chart (e.g., Shewhart or Levey–Jennings chart)
67
Replicate measurements
68
Running replicates
69
RA 9165
70
RA 9514
71
Away from air supply vents and diffusers
72
Position equipment and chemicals at least 6 inches (15 cm) inside the hood, Avoid sudden sash movements
73
Located next to an exterior door that remains open frequently
74
At least 15 minutes
75
Strong alkalis
76
Remain clear of all items at all times and be marked with yellow and black floor tape to remind users to keep it clear
77
Carbon dioxide - because it displaces oxygen without conducting electricity
78
Class B - Foam or dry chemical extinguisher
79
Red body with no band
80
Oxygen, fuel, heat
81
To ensure consistent, safe chemical handling and regulatory compliance
82
Alerts personnel to potential hazards and facilitates emergency response
83
PPE serves as the last line of defense and must be supported by systemic controls
84
Flame-resistant lab coat
85
Neoprene gloves and a chemical-resistant lab coat
86
Cryogenic gloves and a flame-resistant lab coat
87
N95 respirator
88
Face shield with goggles and full-face respirator
89
It supplies filtered air continuously while reducing breathing effort
90
Anti-fog goggles
91
Acute toxicity (fatal or toxic)
92
Physical hazard
93
Biosafety cabinet use, sterilization, and waste segregation
94
Flammable, self-reactive substances, and pyrophorics
95
Risk of long-term health effects like cancer or reproductive toxicity
96
Safety Data Sheet
97
FLAM (Flammable)
98
Dead tree and fish — environmental hazard
99
Corrosive chemical that can cause skin burns and eye damage
100
16