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Cites:

Information Journal Paper

Title

Theoretical Investigation of Stereochemistry of Halogen Addition to Alkenes

Pages

  111-117

Abstract

 Formation processes require relatively low energy. The chemical properties of a molecule, whether in configuration or formally, can affect its reactivity. In this study, the reaction of increasing halogens to an Alkene with methyl and carbohydrate substituents in the presence of different nucleobodies, including HCN, HPMe2, and B3LYP / 6-311G and B3LYP / 6-311G (d, p) HPMePh was investigated and the structural optimization and reactivity parameters of the spatial composition were calculated in different reactions. The results showed that the increase in bromine to cyclohexone with methyl substitutions in the nucleophilic environment of HPMePh is more stable.

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    • Cite

    APA: Copy

    RAZAVI, RAZIEH, Zahedifar, Mahbobeh, & AHMADI, SEYED ALI. (2020). Theoretical Investigation of Stereochemistry of Halogen Addition to Alkenes. NASHRIEH SHIMI VA MOHANDESI SHIMI IRAN (PERSIAN), 39(3 (97) ), 111-117. SID. https://sid.ir/paper/410802/en

    Vancouver: Copy

    RAZAVI RAZIEH, Zahedifar Mahbobeh, AHMADI SEYED ALI. Theoretical Investigation of Stereochemistry of Halogen Addition to Alkenes. NASHRIEH SHIMI VA MOHANDESI SHIMI IRAN (PERSIAN)[Internet]. 2020;39(3 (97) ):111-117. Available from: https://sid.ir/paper/410802/en

    IEEE: Copy

    RAZIEH RAZAVI, Mahbobeh Zahedifar, and SEYED ALI AHMADI, “Theoretical Investigation of Stereochemistry of Halogen Addition to Alkenes,” NASHRIEH SHIMI VA MOHANDESI SHIMI IRAN (PERSIAN), vol. 39, no. 3 (97) , pp. 111–117, 2020, [Online]. Available: https://sid.ir/paper/410802/en

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