![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
![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
![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_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
![Some tert-butyl ether is formed in the solvolysis of tert butyl chloride. Where does this product come from (i.e. what is the substrate and what is the nucleophile?) Do you think this Some tert-butyl ether is formed in the solvolysis of tert butyl chloride. Where does this product come from (i.e. what is the substrate and what is the nucleophile?) Do you think this](https://homework.study.com/cimages/multimages/16/solvolysis2770461178301330651.png)