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(a)
Interpretation:
Predict which SN 1 reaction is faster.
Concept introduction:
SN1 reaction is a unimolecular nucleophilic substitution reaction. It is a first-order kinetics and a two-step mechanism in which bond breaking occurs before bond making. The mechanism has two steps. Carbocations are formed as reactive intermediates. The Heterolysis of the C - Br bond forms an intermediate carbocation. This is the rate-determining step because it involves only bond cleavage. The nucleophilic attack the carbocation forms the new bond in the product.
(b)
Interpretation:
Predict which SN 1 reaction is faster.
Concept introduction:
SN1 reaction is a unimolecular nucleophilic substitution reaction. It is a first-order kinetics and a two-step mechanism in which bond breaking occurs before bond making. The mechanism has two steps. Carbocations are formed as reactive intermediates. The Heterolysis of the C - Br bond forms an intermediate carbocation. This is the rate-determining step because it involves only bond cleavage. The nucleophilic attack the carbocation forms the new bond in the product.
(c)
Interpretation:
Predict which SN 1 reaction is faster.
Concept introduction:
SN1 reaction is a unimolecular nucleophilic substitution reaction. It is a first-order kinetics and a two-step mechanism in which bond breaking occurs before bond making. The mechanism has two steps. Carbocations are formed as reactive intermediates. The Heterolysis of the C - Br bond forms an intermediate carbocation. This is the rate-determining step because it involves only bond cleavage. The nucleophilic attack the carbocation forms the new bond in the product.
(c)
Interpretation:
Predict which SN 1 reaction is faster.
Concept introduction:
SN1 reaction is a unimolecular nucleophilic substitution reaction. It is a first-order kinetics and a two-step mechanism in which bond breaking occurs before bond making. The mechanism has two steps. Carbocations are formed as reactive intermediates. The Heterolysis of the C - Br bond forms an intermediate carbocation. This is the rate-determining step because it involves only bond cleavage. The nucleophilic attack the carbocation forms the new bond in the product.
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Chapter 7 Solutions
Organic Chemistry-Package(Custom)
- Which reaction is fastest out of each pairarrow_forward2) Use your understanding of reaction rates to identify the faster reaction for each of the following pairings. HC Br O CECH Br 2 equiv of OR H NH2 Br 2 equiv of ONH2 Brarrow_forwardExplain why ethene does not react with HX ( X=Cl , Br or I) under normal conditions.arrow_forward
- 2. A reaction similar to #1 is below, however it reacts at a much slower rate, give 2 reasons why and explain. Br ОН 0 °Carrow_forwardWhat reaction out of each pair is faster (SN2 reaction help plz)arrow_forwardWhich SN2 reaction will occur most rapidly? (Assume the concentrations and temperatures are all the same.) * CH;0 + ^CI CH3 + CI- CH, B CH,0 + CH + F CH,O + CH, CH,O Br Br Darrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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