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  • Naming Complex Substituents — Organic Chemistry Tutor
    Organic Chemistry Nomenclature of Organic Compounds Naming Complex Substituents This is the second version of the tutorial on the complex substituents I also have another one in the nomenclature of alkanes and cycloalkanes In this tutorial, I want to talk about the nomenclature of the complex substituents In the last tutorial of this series, we
  • Nomenclature of Alkanes and Cycloalkanes - Organic Chemistry Tutor
    Nomenclature of alkanes and cycloalkanes is one of the fundamental must-know topics for the ACS, MCAT, DAT and other exams
  • Nomenclature of Aldehydes and Ketones - Organic Chemistry Tutor
    The prefix form for carbonyls is “oxo” and it’s going to follow all the same rules as any other substituent which you might have in your molecule For instance, these two molecules are: 4-oxopentanal on the left, and 2-ethyl-4-methyl-3-oxopentanal on the right In terms of priority, aldehydes and ketones are above alcohols and pi-bonds
  • Axial Leaving Group Reactivity — Organic Chemistry Tutor
    In this tutorial, we’ll explore how to analyze chair conformations to predict the outcomes of common organic reactions, such as S N 2 and E2 Using a typical exam question as our starting point, we’ll examine how the positioning of substituents in six-membered rings—specifically in axial or equatorial positions—impacts the reactivity of leaving groups and the accessibility of reaction
  • Nomenclature of Carboxylic Acids — Organic Chemistry Tutor
    Organic Chemistry Nomenclature of Organic Compounds Nomenclature of Carboxylic Acids In this tutorial, I want to talk about the nomenclature of carboxylic acids Let’s start by looking at this molecule over here The molecule has one, two, three carbon atoms, which means that the parent name, or the principal chain, is going to be propane
  • Nomenclature of Alkenes and Cycloalkenes - Organic Chemistry Tutor
    For cyclic compounds, choose the carbon of the C=C that leads to the shortest route to the next substituent or double bond Fun Fact: The numbering system in organic nomenclature was designed for clarity and consistency, ensuring scientists across the globe speak the same ‘chemical language’
  • Birch Reduction — Organic Chemistry Tutor
    The Birch reduction is one of the few reactions that destroy aromaticity and make a substituted 1,4-cyclohexadienes
  • Intramolecular Aldol Condensation — Organic Chemistry Tutor
    Intramolecular aldol condensation is a tricky topic In this tutorial I'll walk you through several examples and show you how to tackle them!
  • Aromatic Compounds and Aromaticity - Organic Chemistry Tutor
    Organic Chemistry Aromatic Compounds and Aromaticity In this lesson we are going to explore the phenomenon of aromaticity and related topics Reactions of Aromatic Compounds (Overview) Aromatic compounds are incredibly important in organic chemistry and targeted organic synthesis They are also incredibly versatile in terms of the transformations they go through Finally, they show up
  • Nomenclature of Alcohols — Organic Chemistry Tutor
    This gives us a butyl substituent at carbon 2 and two methyl groups at carbon 5 Alphabetizing these substituents gives the name 2-butyl-5,5-dimethylcyclohexanol





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