![Write a mechanism for the reaction of tert-butyl alcohol with concentrated HCL. | Homework.Study.com Write a mechanism for the reaction of tert-butyl alcohol with concentrated HCL. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screen_shot_2021-02-21_at_2.16.07_pm7741377435796410486.png)
Write a mechanism for the reaction of tert-butyl alcohol with concentrated HCL. | Homework.Study.com
![53001-22-2 | tert-Butyl Alcohol-d10 | 2-Methyl-2-propanol-d10; tert-Butanol-d10; 2-(Methyl-d3)-2-propan-1,1,1,3,3,3-d6-ol-d; Trimethylcarbinol-d10; Trimethylmethanol-d10; t-Butanol-d10; | C₄D₁₀O | TRC 53001-22-2 | tert-Butyl Alcohol-d10 | 2-Methyl-2-propanol-d10; tert-Butanol-d10; 2-(Methyl-d3)-2-propan-1,1,1,3,3,3-d6-ol-d; Trimethylcarbinol-d10; Trimethylmethanol-d10; t-Butanol-d10; | C₄D₁₀O | TRC](https://www.trc-canada.com/prod-img/T117541.png)
53001-22-2 | tert-Butyl Alcohol-d10 | 2-Methyl-2-propanol-d10; tert-Butanol-d10; 2-(Methyl-d3)-2-propan-1,1,1,3,3,3-d6-ol-d; Trimethylcarbinol-d10; Trimethylmethanol-d10; t-Butanol-d10; | C₄D₁₀O | TRC
![t-butyl alcohol reacts less rapidly with metalic sodium than the primary alcohol. Explain why? - YouTube t-butyl alcohol reacts less rapidly with metalic sodium than the primary alcohol. Explain why? - YouTube](https://i.ytimg.com/vi/db2sLfAjrB8/maxresdefault.jpg)
t-butyl alcohol reacts less rapidly with metalic sodium than the primary alcohol. Explain why? - YouTube
When the vapours of tertiary butyl alcohol are passed through heated copper at 573 K , the product formed is:
![Alkylation of Phenol with Tertiary Butyl Alcohol over Zeolites | Organic Process Research & Development Alkylation of Phenol with Tertiary Butyl Alcohol over Zeolites | Organic Process Research & Development](https://pubs.acs.org/cms/10.1021/op010077n/asset/images/large/op010077nn00001.jpeg)