Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud

The focus of this study is to synthesize the naphthoquinone derivative via the reaction of pyridinium salt with methyl naphthoquinone. The starting material 2,4-dibromoacetophenone reacted with pyridine to produce pyridinium salt in 96.29% yield. The further reaction was done, producing naphthoquino...

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Main Author: Mohamed Daud, Nor Shazana
Format: Thesis
Language:English
Published: 2010
Online Access:https://ir.uitm.edu.my/id/eprint/102128/1/102128.pdf
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spelling my-uitm-ir.1021282024-09-12T03:22:13Z Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud 2010 Mohamed Daud, Nor Shazana The focus of this study is to synthesize the naphthoquinone derivative via the reaction of pyridinium salt with methyl naphthoquinone. The starting material 2,4-dibromoacetophenone reacted with pyridine to produce pyridinium salt in 96.29% yield. The further reaction was done, producing naphthoquinone derivative in 25.71% yield in the mixture of isomer red and yellow compounds. The product consists isomer of two compounds was separated using column chromatography. The isolated red and yellow compounds was characterized using IR and NMR analysis. The study on the times of refluxing was also performed in order to determine the optimum time of salt formation. The formation of pyridinium salt is directly proportional with time of refluxing. 2010 Thesis https://ir.uitm.edu.my/id/eprint/102128/ https://ir.uitm.edu.my/id/eprint/102128/1/102128.pdf text en public degree Universiti Teknologi MARA (UiTM) Faculty of Applied Sciences Abdullah, Noraishah Micheal, Allan Abdul Ghani, Fazni Susila
institution Universiti Teknologi MARA
collection UiTM Institutional Repository
language English
advisor Abdullah, Noraishah
Micheal, Allan
Abdul Ghani, Fazni Susila
description The focus of this study is to synthesize the naphthoquinone derivative via the reaction of pyridinium salt with methyl naphthoquinone. The starting material 2,4-dibromoacetophenone reacted with pyridine to produce pyridinium salt in 96.29% yield. The further reaction was done, producing naphthoquinone derivative in 25.71% yield in the mixture of isomer red and yellow compounds. The product consists isomer of two compounds was separated using column chromatography. The isolated red and yellow compounds was characterized using IR and NMR analysis. The study on the times of refluxing was also performed in order to determine the optimum time of salt formation. The formation of pyridinium salt is directly proportional with time of refluxing.
format Thesis
qualification_level Bachelor degree
author Mohamed Daud, Nor Shazana
spellingShingle Mohamed Daud, Nor Shazana
Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
author_facet Mohamed Daud, Nor Shazana
author_sort Mohamed Daud, Nor Shazana
title Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
title_short Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
title_full Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
title_fullStr Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
title_full_unstemmed Synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / Nor Shazana Mohamed Daud
title_sort synthesis of naphthoquinone derivatives with some study on percentage rate of formation for pyridinium salt / nor shazana mohamed daud
granting_institution Universiti Teknologi MARA (UiTM)
granting_department Faculty of Applied Sciences
publishDate 2010
url https://ir.uitm.edu.my/id/eprint/102128/1/102128.pdf
_version_ 1811769212131082240