![organic chemistry - Why is the reaction rate of tert-butyl chloride solvolysis faster in 80% water/20% acetone, than in 70% water/30% acetone? - Chemistry Stack Exchange organic chemistry - Why is the reaction rate of tert-butyl chloride solvolysis faster in 80% water/20% acetone, than in 70% water/30% acetone? - Chemistry Stack Exchange](https://i.stack.imgur.com/7RlnJ.png)
organic chemistry - Why is the reaction rate of tert-butyl chloride solvolysis faster in 80% water/20% acetone, than in 70% water/30% acetone? - Chemistry Stack Exchange
![What is order reactivity of SN1 and SN2 of n-butyl chloride, n-butyl bromide, sec-butyl chloride, tert-butyl chloride, and crotyl chloride. Why? | Homework.Study.com What is order reactivity of SN1 and SN2 of n-butyl chloride, n-butyl bromide, sec-butyl chloride, tert-butyl chloride, and crotyl chloride. Why? | Homework.Study.com](https://homework.study.com/cimages/multimages/16/capture28-97700687943462451283.jpg)
What is order reactivity of SN1 and SN2 of n-butyl chloride, n-butyl bromide, sec-butyl chloride, tert-butyl chloride, and crotyl chloride. Why? | Homework.Study.com
![A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11144-020-01723-w/MediaObjects/11144_2020_1723_Sch1_HTML.png)
A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink
![A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11144-020-01723-w/MediaObjects/11144_2020_1723_Fig10a_HTML.png)
A solvent-catalyzed four-molecular two-path solvolysis mechanism of t-butyl chloride or bromide in water or alcohol derived by density functional theory calculation and confirmed by high-resolution electrospray ionization-mass spectrometry | SpringerLink
![Is the tert-Butyl Chloride Solvolysis the Most Misunderstood Reaction in Organic Chemistry? Evidence Against Nucleophilic Solvent Participation in the tert-Butyl Chloride Transition State and for Increased Hydrogen Bond Donation to the 1-Adamantyl Is the tert-Butyl Chloride Solvolysis the Most Misunderstood Reaction in Organic Chemistry? Evidence Against Nucleophilic Solvent Participation in the tert-Butyl Chloride Transition State and for Increased Hydrogen Bond Donation to the 1-Adamantyl](https://pubs.acs.org/cms/10.1021/ja010600d/asset/images/medium/ja010600dh00002.gif)