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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
The complex methylene pmr spectra of some a- dinitrophenyl-Ş- keto esters is explained in terms of chirality of the molecules due to hindered rotation about aromatic carbon-aliphatic carbon bond. pmr and cmr data is reported in order to prove the conc- luisons.
📌 3 Key Takeaways
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Objective & Hypothesis:The complex methylene pmr spectra of some a- dinitrophenyl-Ş- keto esters is explained in terms of chirality of the molecules due to hindered rotation about aromatic carbon-aliphatic carbon bond. pmr and cmr data is reported in order to prove the conc- luisons.
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Key Findings & Data:The complex methylene pmr spectra of some a- dinitrophenyl-Ş- keto esters is explained in terms of chirality of the molecules due to hindered rotation about aromatic carbon-aliphatic carbon bond. pmr and cmr data is reported in order to prove the conc- luisons.
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Conclusion & Impact:The complex methylene pmr spectra of some a- dinitrophenyl-Ş- keto esters is explained in terms of chirality of the molecules due to hindered rotation about aromatic carbon-aliphatic carbon bond. pmr and cmr data is reported in order to prove the conc- luisons.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Chirality · Dinitrophenyl · Keto Esters
Abstract
The complex methylene pmr spectra of some a- dinitrophenyl-Ş- keto esters is explained in terms of chirality of the molecules due to hindered rotation about aromatic carbon-aliphatic carbon bond. pmr and cmr data is reported in order to prove the conc- luisons.
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Cite This Article
ERK, Ç. (1978). Chirality in a- Dinitrophenyl -p- Keto Esters. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering, Cilt: 24, 1–1. https://ajindex.com/articles/810246