Summary: Introduction To Organic Chemistry | William H Brown, et al
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Read the summary and the most important questions on Introduction to Organic Chemistry | William H. Brown; Thomas Poon
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1 Covalent Bonding and Shapes of Molecules
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1.1 How do we Describe the Electronic Structures of Atoms?
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What are the principle energy levels?
The principle energy levels are the space to which an electron in confined to move within. -
How are electrons further grouped?
1. The principle energy levels or Shells.
2. The subshells s, p, d and f.
3. Orbitals, each containing a maximum of 2 electrons -
How are the orbitals distributed within the shells?
1. 1 s orbital in each shell
2. 3 p orbitals in each shell, except the first shell
3. 5 d orbitals in each shell, except the first two shells
4. 7 f orbitals in each shell, except the first three shells -
What are the first 10 elements of the periodic table?
Hydrogen, Helium, Lithium, Berylium, Boor, Carbon, Nitrogen, Oxygen, Fluor, Neon -
What is the element of the periodic table with atomic number 8? And what is the electron configuration?
Oxygen, 1s2 2s2 2px2 2py1 2pz1 -
What is a lewis structure?
A representation of an electron with it's valence electrons drawn. -
1.2 What is the Lewis Model of Bonding?
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How is an ionic bond formed?
An ionic bond is formed when an electron transfers from the valence shell of an atom with lower electronegativity to one with higher electronegativity. -
When does ionic transfer of electrons occur?
The guideline is when the difference in electronegativity is 1,9 or greater. -
What is a dipole and how can you display this?
A dipole is when there is a seperation of charge within a covalent bond or molecule. This can be displayed in a electron density model, with blue showing the more negative part and red the more positive part. -
What is the formal charge and how to derive it?
The formal charge is the charge on an atom or molecule and can be derived by:
1. Writing down the Lewis structure.
2. Assign al unshared electrons.
3. Compare the number of electrons with the number of electrons in the neutral, unbonded atom.
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Topics related to Summary: Introduction To Organic Chemistry
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Covalent Bonding and Shapes of Molecules
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Acids and Bases - What are the Relationships between Acidity and Molecular Structure?
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Alkanes and Cycloalkanes - What are Alkanes?
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Alkanes and Cycloalkanes - How do we name Alkanes?
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Alkanes and Cycloalkanes - What are the Conformations of Alkanes and Cycloalkanes?
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Alkanes and Cycloalkanes - What are the Physical Properties of Alkanes and Cycloalkanes?
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Alkenes and Alkynes - What are the Structures and Shapes of Alkenes and Alkynes?
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Alkenes and Alkynes - How do we Name Alkenes and Alkynes?
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Reactions of Alkenes and Alkynes - What is a Reaction Mechanism?
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Reactions of Alkenes and Alkynes - What are the Mechanisms of Electrophilic Addition to Alkenes?
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Reactions of Alkenes and Alkynes - What are Carbocation Rearrangements?
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Reactions of Alkenes and Alkynes - What is Hydroboration-Oxidation of Alkene?
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Reactions of Alkenes and Alkynes - How can an Alkene be Reduced to an Alkane?
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Chirality: The Handedness of Molecules - What are Enantiomers?
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Chirality: The Handedness of Molecules - How do we Designate the Configuration of a Stereocenter?
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Chirality: The Handedness of Molecules - What is the 2n Rule?
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Chirality: The Handedness of Molecules - How is Chirality detected in the Laboratory?
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Haloalkanes - How are Haloalkanes Named?
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Haloalkanes - What Are the SN2 and SN1 Mechanisms for Nucleophilic Substitution?
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Haloalkanes - What Determines Whether SN1 or SN2 Predominates?
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Haloalkanes - When Do Nucleophilic Substitution and beta-Elimination Compete?
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Alcohols, Ethers, and Thiols - What Are Alcohols?
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Alcohols, Ethers, and Thiols - What Are the Characteristic Reactions of Alcohols?
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Alcohols, Ethers, and Thiols - What Are Ethers?
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Alcohols, Ethers, and Thiols - What Are Epoxides?
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Benzene and Its Derivatives - What Is the Structure of Benzene?
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Benzene and Its Derivatives - How Are Benzene Compounds Named, and What Are Their Physical Properties?
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Benzene and Its Derivatives - What Is the Benzylic Position, and How Does It Contribute to Benzene Reactivity?
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Benzene and Its Derivatives - What Is the Mechanism of Electrophilic Aromatic Substitution?
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Benzene and Its Derivatives - How Do Existing Substituents on Benzene Affect Electrophilic Aromatic Substitution?
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Aldehydes and Ketones - How Are Aldehydes and Ketones Named?
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Aldehydes and Ketones - What Are Grignard Reagents, and How Do They React with Aldehydes and Ketones?
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Aldehydes and Ketones - What Are Hemiacetals and Acetals?
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Aldehydes and Ketones - How Do Aldehydes and Ketones React with Ammonia and Amines?
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Aldehydes and Ketones - What Is Keto–Enol Tautomerism?
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Aldehydes and Ketones - How Are Aldehydes and Ketones Oxidized?
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Aldehydes and Ketones - How Are Aldehydes and Ketones Reduced?
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Carboxylic Acids - How Are Carboxylic Acids Named?
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Carboxylic Acids - What Are the Physical Properties of Carboxylic Acids?
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Carboxylic Acids - What Are the Acid–Base Properties of Carboxylic Acids?
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Carboxylic Acids - How Are Carboxyl Groups Reduced?
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Carboxylic Acids - What Is Fischer Esterification?
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Carboxylic Acids - What are Acid Chlorides?
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Carboxylic Acids - What Is Decarboxylation?