which one is the most reactive towards sn1 reaction ?

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Which one is most reactive towards SN 1 reaction?A. C 6 H 5 CH … – BYJU’S
The correct option is D C6H5C (CH3) (C6H5)Br Reactivity in reactions depends upon the stability of the carbocation intermediate. Since the stability of the carbocations increases in order: Therefore, the alkyl halide C6H5C (CH3) (C6H5) is the most reactive. Suggest Corrections 73 Similar questions Q.

https://chem.libretexts.org/Courses/Brevard_College/CHE_202:_Organic_Chemistry_II/04:_Substitution_and_Elimination_reactions/4.07:_Factors_Affecting_the_SN1_Reaction

https://chem.libretexts.org/Courses/Brevard_College/CHE_202:_Organic_Chemistry_II/04:_Substitution_and_Elimination_reactions/4.07:_Factors_Affecting_the_SN1_Reaction
4.7: Factors Affecting the SN1 Reaction – Chemistry LibreTexts
Brevard College CHE 202: Organic Chemistry II 4: Substitution and Elimination reactions

https://chem.libretexts.org / Bookshelves / Organic_Chemistry / Organic_Chemistry_I_(Liu) / 07:_Nucleophilic_Substitution_Reactions / 7.04:_SN1_Reaction_Mechanism_Energy_Diagram_and_Stereochemistry

https://chem.libretexts.org / Bookshelves / Organic_Chemistry / Organic_Chemistry_I_(Liu) / 07:_Nucleophilic_Substitution_Reactions / 7.04:_SN1_Reaction_Mechanism_Energy_Diagram_and_Stereochemistry
7.4: SN1 Reaction Mechanism, Energy Diagram and Stereochemistry
16 déc. 2021Bookshelves Organic Chemistry Organic Chemistry I (Liu) 7: Nucleophilic Substitution Reactions

https://kpu.pressbooks.pub/organicchemistry/chapter/7-4-sn1-reaction-mechanism-energy-diagram-and-stereochemistry

https://kpu.pressbooks.pub/organicchemistry/chapter/7-4-sn1-reaction-mechanism-energy-diagram-and-stereochemistry
7.4 SN1 Reaction Mechanisms, Energy Diagram and Stereochemistry
Introduction Acknowledgements Chapter 1: Basic Concepts in Chemical Bonding and Organic Molecules 1.1 Chemical Bonding 1.2 Lewis Structure 1.3 Resonance Structures 1.4 Resonance Structures in Organic Chemistry 1.5 Valence-Shell Electron-Pair Repulsion Theory (VSEPR) 1.6 Valence Bond Theory and Hybridization Answers to Chapter 1 Practice Questions

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.05:_Characteristics_of_the_SN1_Reaction

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.05:_Characteristics_of_the_SN1_Reaction
11.5: Characteristics of the SN1 Reaction – Chemistry LibreTexts
Organic Chemistry Organic Chemistry (Morsch et al.) 11: Reactions of Alkyl Halides- Nucleophilic Substitutions and Eliminations

https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.13:_A_Summary_of_Reactivity_-_SN1_SN2_E1_E1cB_and_E2

https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.13:_A_Summary_of_Reactivity_-_SN1_SN2_E1_E1cB_and_E2
11.13: A Summary of Reactivity – SN1, SN2, E1, E1cB, and E2
15 janv. 2023The next most import variable for predicting the outcome of a reaction is the nature of the nucleophilic reactant. Strong nucleophiles favor S N 2 substitution, and strong bases, especially strong hindered bases (such as tert-butoxide) favor E2 elimination. Weak nucleophiles that are also weak bases tend to favor S N 1 and E1 .

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.04:_The_SN1_Reaction

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/11:_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.04:_The_SN1_Reaction
11.4: The SN1 Reaction – Chemistry LibreTexts
The S N 1 mechanism. A second model for a nucleophilic substitution reaction is called the ‘dissociative’, or ‘S N 1’ mechanism. In the S N 1 reaction, the bond between the substrate and the leaving group is broken when the leaving group departs with the pair of electrons that formerly composed the bond.. This results in the formation of a carbocation (from carbon and cation) the word for …

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Substitution_Reactions/SN1/SN1_Reaction

https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Substitution_Reactions/SN1/SN1_Reaction
SN1 Reaction – Chemistry LibreTexts
23 janv. 2023Organic Chemistry Supplemental Modules (Organic Chemistry) Reactions

https://www.chemistrylearner.com/sn1-reaction.html

https://www.chemistrylearner.com/sn1-reaction.html
SN1 Reaction: Definition, Example, and Mechanism – Chemistry Learner
Characteristics of SN1 Reaction. Two-step reaction process: 1. carbon-halogen bond breaks, resulting in a positively charged carbon (carbocation) and 2. nucleophile attacks the carbocation, forming a new bond. Unimolecular and follows first-order kinetics. Rate of the reaction depends on the concentration of the substrate (alkyl halide)

https://chemistry.stackexchange.com/questions/51043/reactivity-towards-sn1-reaction

https://chemistry.stackexchange.com/questions/51043/reactivity-towards-sn1-reaction
Reactivity towards SN1 reaction – Chemistry Stack Exchange
Reactivity towards SN1 reaction. In the following compounds , we have to find order of compounds of their reactivity towards SN1 reaction. According to me , we should compare carbo cation stability which is formed as an intermediate. So the 4th compound (tertiary butyl chloride) should be in top in order of reactivity. lesoutrali bot