![Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screenshot_2022-06-25_at_10.47.32_pm6211904680490769642.png)
Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. | Homework.Study.com
![Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0009250921003110-gr9.jpg)
Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect
Regiodivergent Reductive Opening of Epoxides by Catalytic Hydrogenation Promoted by a (Cyclopentadienone)iron Complex | ACS Catalysis
![Predict the major product when the below-mentioned steroidal epoxide is treated with LiAlH4. | Homework.Study.com Predict the major product when the below-mentioned steroidal epoxide is treated with LiAlH4. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/ligjkk8825355052983611708.png)