Reactivity 3.4.2—In a nucleophilic substitution reaction, a nucleophile donates an electron pair to form a new bond, as another bond breaks producing a leaving group. Deduce equations with descriptions and explanations of the movement of electron pairs in nucleophilic substitution reactions.
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[N/A]Directly related questions
- 19M.1A.HL.TZ2.25: Which of the following can be both formed from bromoethane and converted directly into...
- 19M.1A.HL.TZ2.25: Which of the following can be both formed from bromoethane and converted directly into...
- 19M.1A.HL.TZ2.25: Which of the following can be both formed from bromoethane and converted directly into...
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19M.2.SL.TZ2.6e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
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19M.2.SL.TZ2.6e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
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19M.2.SL.TZ2.e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
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19M.2.SL.TZ2.6e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
-
19M.2.SL.TZ2.6e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
-
19M.2.SL.TZ2.e:
The minor product, C6H5–CH2–CH2Br, can be directly converted to an intermediate compound, X, which can then be directly converted to the acid C6H5–CH2–COOH.
C6H5–CH2–CH2Br → X → C6H5–CH2–COOH
Identify X.
- 19N.1A.SL.TZ0.26: What type of reaction occurs when C6H13Br becomes C6H13OH? A. Nucleophilic substitution B. ...
- 19N.1A.SL.TZ0.26: What type of reaction occurs when C6H13Br becomes C6H13OH? A. Nucleophilic substitution B. ...
- 19N.1A.SL.TZ0.26: What type of reaction occurs when C6H13Br becomes C6H13OH? A. Nucleophilic substitution B. ...
- 19N.1A.SL.TZ0.26: What type of reaction occurs when C6H13Br becomes C6H13OH? A. Nucleophilic substitution B. ...
- 22M.1A.SL.TZ1.27: What is produced when chlorobutane is treated with aqueous sodium hydroxide solution? A. ...
- 22M.1A.SL.TZ1.27: What is produced when chlorobutane is treated with aqueous sodium hydroxide solution? A. ...
- 22M.1A.SL.TZ1.27: What is produced when chlorobutane is treated with aqueous sodium hydroxide solution? A. ...
- 22M.1A.SL.TZ1.27: What is produced when chlorobutane is treated with aqueous sodium hydroxide solution? A. ...
- 22M.1A.SL.TZ2.27: Which reaction mechanisms are typical for alcohols and halogenoalkanes?
- 22M.1A.SL.TZ2.27: Which reaction mechanisms are typical for alcohols and halogenoalkanes?
- 22M.1A.SL.TZ2.27: Which reaction mechanisms are typical for alcohols and halogenoalkanes?
- 22M.1A.SL.TZ2.27: Which reaction mechanisms are typical for alcohols and halogenoalkanes?
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22M.2.SL.TZ1.6a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.
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22M.2.SL.TZ1.6a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.
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22M.2.SL.TZ1.a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.
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22M.2.SL.TZ1.6a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.
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22M.2.SL.TZ1.6a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.
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22M.2.SL.TZ1.a(iii):
Explain the relative lengths of the three bonds between N and O in nitric acid.