![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)
Alkylation of Phenol with Tertiary Butyl Alcohol over Zeolites | Organic Process Research & Development
Assertion: Tert. butyl alcohol on heating with conc. H2SO4 at 413 K gives 2 methyl propane as the main product and not di tert. butyl ether. Reason: All alcohols are readily dehydrated
![Which of the following pairs of compounds are position isomers?A.Isobutyl alcohol and s-butyl alcoholB.Isobutyl alcohol and t-butyl alcoholC.Isobutyl alcohol and neo-pentyl alcoholD.Ethyl alcohol and ethylene glycol Which of the following pairs of compounds are position isomers?A.Isobutyl alcohol and s-butyl alcoholB.Isobutyl alcohol and t-butyl alcoholC.Isobutyl alcohol and neo-pentyl alcoholD.Ethyl alcohol and ethylene glycol](https://www.vedantu.com/question-sets/84cfbfa3-77c8-4b34-a7b6-37d6e7c390a98499045297205226264.png)
Which of the following pairs of compounds are position isomers?A.Isobutyl alcohol and s-butyl alcoholB.Isobutyl alcohol and t-butyl alcoholC.Isobutyl alcohol and neo-pentyl alcoholD.Ethyl alcohol and ethylene glycol
When the vapours of tertiary butyl alcohol are passed through heated copper at 573 K , the product formed is:
![75-65-0 | Tert-butyl Alcohol | 1,1-Dimethylethanol; 2-Methyl-2-propanol; Trimethylcarbinol; Trimethylmethanol; t-Butanol; tert-Butanol | C₄H₁₀O | TRC 75-65-0 | Tert-butyl Alcohol | 1,1-Dimethylethanol; 2-Methyl-2-propanol; Trimethylcarbinol; Trimethylmethanol; t-Butanol; tert-Butanol | C₄H₁₀O | TRC](https://www.trc-canada.com/prod-img/T117540.png)
75-65-0 | Tert-butyl Alcohol | 1,1-Dimethylethanol; 2-Methyl-2-propanol; Trimethylcarbinol; Trimethylmethanol; t-Butanol; tert-Butanol | C₄H₁₀O | 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 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
![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)