Inorganic Chemistry Archives

Posted inin Inorganic Chemistry

Benzene Carboxylic Acid vs Ethanoic Acid: Understanding Acid Strength Factors

Posted byby Franklin Veaux
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3 min

Why is Benzene Carboxylic Acid Stronger than Ethanoic Acid? Benzene carboxylic acid (benzoic acid) shows stronger acidity than ethanoic acid due to multiple factors: the hybridization of the adjacent carbon,...

Posted inin Inorganic Chemistry

Which is More Basic? A Guide to Understanding Basicity in Chemistry and Language

Posted byby Franklin Veaux
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7 min

Which is More Basic? Understanding Basicity in Chemistry Determining which species is more basic depends on the stability of its conjugate acid and conjugate base, resonance effects, charge localization, and...

Posted inin Inorganic Chemistry

Understanding the Acronym B.R.S.M in Chemistry: Meaning and Controversies Explained

Posted byby Franklin Veaux
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2 min

Understanding the Acronym “B.R.S.M” in Chemistry “B.R.S.M” stands for “Based on Recovered Starting Material.” It is a yield calculation metric used in synthetic chemistry. The term indicates that the percentage...

Posted inin Inorganic Chemistry

Grignard Reagent and Gilman Reagent: Nucleophilicity, Reactivity, and Applications

Posted byby Franklin Veaux
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1 min

Grignard Reagent vs Gilman Reagent Grignard reagents and Gilman reagents differ mainly in nucleophilicity, selectivity, and reactivity, influencing how each behaves in organic synthesis. 1. Nucleophilicity and Selectivity Gilman reagents...

Posted inin Inorganic Chemistry

How to Read NMR: A Guide to Interpreting Proton Signals and Chemical Shifts

Posted byby Franklin Veaux
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2 min

How to Read NMR Reading Nuclear Magnetic Resonance (NMR) spectroscopy involves interpreting proton signals (H1 NMR) based on chemical shifts, splitting patterns, and integration of peaks to deduce molecular structure....

Posted inin Inorganic Chemistry

Visualizing Stereochemistry in Sharpless Asymmetric Epoxidation: A Clear Guide

Posted byby Franklin Veaux
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2 min

Visualizing Sharpless Asymmetric Epoxidation Stereochemistry The best way to visualize how Sharpless asymmetric epoxidation works stereochemically is by using the “left hand rule” mnemonic, which helps predict the stereochemical outcome...

Posted inin Inorganic Chemistry

The Debate Over Using “Orgo” for Organic Chemistry: Perspectives and Alternatives

Posted byby Franklin Veaux
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7 min

Discussion: The Preference Against Calling Organic Chemistry “Orgo” Some students and professionals prefer not to call organic chemistry “orgo” because they find the term unintuitive, linguistically unclear, and socially awkward;...

Posted inin Inorganic Chemistry

Master Organic Chemistry: Analyzing Its Value and Effective Study Strategies

Posted byby Franklin Veaux
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3 min

Master Organic Chemistry: Is It Worth It? Master Organic Chemistry is a valuable supplementary resource, but not absolutely necessary to excel in organic chemistry. Students who use it actively—by creating...

Posted inin Inorganic Chemistry

How This Reaction Forms a Tert-Butyl Group Instead of an Isobutyl Group

Posted byby Franklin Veaux
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2 min

Why Does This Reaction Add a Tert-Butyl Group Instead of an Isobutyl Group? The reaction adds a tert-butyl group instead of an isobutyl group because the initially formed primary carbocation...

Posted inin Inorganic Chemistry

Synthesis and Characteristics of Light Yellow Benzil Crystals from Benzoin Oxidation

Posted byby Franklin Veaux
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5 min

Crystals of Benzil: Synthesis and Characteristics Benzil forms as light yellow colored crystalline solid through the oxidation of benzoin. The typical synthesis involves oxidizing benzoin using a strong oxidizing agent....