Organic Chemistry - Unit 1

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Questions and Answers

What is the main product formed when propene reacts with HCl in a hydrohalogenation reaction?

  • Propanol
  • Propane
  • 1-Chloropropane (correct)
  • 2-Chloropropane

Which of the following functional groups is NOT present in the compound CH3CH2CH2NH2?

  • Alkyl halide (correct)
  • Alkane
  • Alcohol
  • Amine

In a nucleophilic substitution reaction, what is the general role of the nucleophile?

  • To act as a catalyst for the reaction
  • To break the bond between the leaving group and the substrate
  • To accept a pair of electrons from the electrophile
  • To donate a pair of electrons to the electrophile (correct)

Which of the following is NOT a characteristic of addition polymers?

<p>Formed from two different types of monomers (D)</p> Signup and view all the answers

What type of product is formed in a nucleophilic substitution reaction involving an alkyl halide?

<p>An alcohol (D)</p> Signup and view all the answers

Which of the following monomers would be used to make a polymer through addition polymerization?

<p>Ethylene (CH2=CH2) (B)</p> Signup and view all the answers

Which functional group is commonly found in both esters and carboxylic acids?

<p>-C=O (B)</p> Signup and view all the answers

Which of the following statements correctly describes the relationship between monomers and polymers?

<p>Monomers are small molecules that are linked together to form larger polymers (B)</p> Signup and view all the answers

What does the Quantum Mechanical Model of the atom primarily describe about electrons?

<p>Electrons are positioned in probability clouds called orbitals. (C)</p> Signup and view all the answers

Which principle states that the exact position and momentum of an electron cannot be known simultaneously?

<p>Heisenberg Uncertainty Principle (C)</p> Signup and view all the answers

Which molecular shape is associated with four electron pairs in VSEPR theory?

<p>Tetrahedral (A)</p> Signup and view all the answers

How does raising the temperature affect the equilibrium constant (K) for an endothermic reaction?

<p>Increases K (D)</p> Signup and view all the answers

Which of the following shapes corresponds to three bonding electron pairs and one lone pair?

<p>Trigonal Pyramidal (C)</p> Signup and view all the answers

In the context of VSEPR theory, what molecular shape results from five bonding pairs of electrons?

<p>Trigonal Bipyramidal (D)</p> Signup and view all the answers

What effect does a catalyst have on a chemical reaction?

<p>Speeds up the reaction without being consumed. (C)</p> Signup and view all the answers

What is the bond angle in a molecule with a Tetrahedral shape?

<p>109.5° (C)</p> Signup and view all the answers

What is the electron configuration of the Cu2+ cation?

<p>[Ar] 3d9 (B)</p> Signup and view all the answers

Which type of intermolecular force is present in all molecules?

<p>London Dispersion Forces (C)</p> Signup and view all the answers

Which condition indicates a molecule is polar based on its molecular structure?

<p>Asymmetrical geometry with differing electronegativities (A)</p> Signup and view all the answers

What is the strongest type of intermolecular force listed?

<p>Hydrogen Bonds (C)</p> Signup and view all the answers

Which of the following is a characteristic of nonpolar molecules?

<p>They have symmetrical geometry. (C)</p> Signup and view all the answers

What is true about the boiling points of molecules with stronger intermolecular forces?

<p>They have higher boiling points. (A)</p> Signup and view all the answers

For a molecule to be considered polar, what must the difference in electronegativity typically be?

<p>Between 0.5 and 2.0 (B)</p> Signup and view all the answers

Which type of molecule would typically show higher solubility in water?

<p>Polar molecules capable of hydrogen bonding (A)</p> Signup and view all the answers

What is the correct product when a primary alcohol undergoes oxidation?

<p>Aldehyde (C)</p> Signup and view all the answers

Which functional group is present in Carboxylic Acids?

<p>Carboxyl group (-COOH) (A)</p> Signup and view all the answers

Which reaction type results in the conversion of alkenes to alkanes?

<p>Hydrogenation (C)</p> Signup and view all the answers

What is produced when a secondary alcohol is oxidized?

<p>Ketone (C)</p> Signup and view all the answers

Which of the following compounds contains a carbonyl group?

<p>Acetamide (B)</p> Signup and view all the answers

Which functional group is represented by (-COO-)?

<p>Ester (A)</p> Signup and view all the answers

What is the result of the halogenation reaction involving alkenes?

<p>Formation of dihalides (C)</p> Signup and view all the answers

Which of the following substances does not undergo oxidation when subjected to oxidizing conditions?

<p>Tertiary Alcohols (D)</p> Signup and view all the answers

What is the effect of a catalyst on the activation energy of a reaction?

<p>It decreases the activation energy. (D)</p> Signup and view all the answers

How do catalysts affect the position of equilibrium in a chemical reaction?

<p>Catalysts have no effect on the position of equilibrium. (A)</p> Signup and view all the answers

Which of the following best describes collision theory?

<p>Reactions occur when molecules collide with sufficient energy and correct orientation. (C)</p> Signup and view all the answers

Which action would shift the equilibrium of an endothermic reaction towards products?

<p>Increasing the temperature. (B)</p> Signup and view all the answers

What role does temperature play in reaction rates according to collision theory?

<p>It increases the energy and frequency of collisions. (B)</p> Signup and view all the answers

In terms of Le Chatelier's Principle, what happens when the concentration of products is decreased in an exothermic reaction?

<p>Equilibrium shifts to the products. (A)</p> Signup and view all the answers

What is ΔH, and how is it influenced by catalysts?

<p>ΔH is the change in enthalpy and is not altered by catalysts. (B)</p> Signup and view all the answers

Which statement correctly identifies the outcome of increased pressure in gaseous reactions?

<p>It shifts equilibrium to the side with fewer moles of gas. (D)</p> Signup and view all the answers

Flashcards

Structural Isomers

Compounds with the same chemical formula but different arrangements of atoms.

Alcohols

Compounds with a hydroxyl (OH) group bonded to a carbon atom.

Aldehydes

Compounds with a carbonyl group (C=O) connected to two other groups.

Ketones

Compounds with a carbonyl group (C=O) connected to one R group and one hydrogen.

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Oxidation of Alcohols

A reaction where electrons are lost. Primary alcohols form aldehydes, secondary alcohols form ketones, and aldehydes form carboxylic acids.

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Hydrogenation

A reaction where hydrogen is added across a double or triple bond. Alkynes and alkenes become alkanes.

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Hydration

A reaction where water is added across a double bond. Alkenes become alcohols.

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Halogenation

A reaction where a halogen atom is added across a double bond. Alkenes become dihalides.

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Hydrohalogenation

A chemical reaction where an alkene reacts with a hydrogen halide (HCl, HBr) to form an alkyl halide.

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Nucleophilic Substitution

A chemical reaction where a nucleophile replaces a halide group (X) in an alkyl halide (R-X).

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Electrophilic Substitution

A chemical reaction where a hydrogen atom in an aromatic compound is replaced by an electrophile.

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Polymer

A large molecule formed by the linking of many smaller repeating units called monomers.

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Monomer

A small molecule that can be linked to other similar molecules to form a polymer.

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Polymerization

The process of linking monomer units together to form a polymer.

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Addition Polymer

A polymer formed by the addition of monomers with double bonds, without any byproducts.

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Condensation Polymer

A polymer formed by the reaction of two or more monomers, with the elimination of small molecules like water or alcohol.

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London Dispersion Forces

The weakest type of intermolecular force present in all molecules, regardless of polarity. These forces are caused by temporary fluctuations in electron distribution, creating temporary dipoles.

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Dipole-Dipole Forces

A type of intermolecular force occurring only in polar molecules. It arises from the attraction between the positive end of one polar molecule and the negative end of another.

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Hydrogen Bonding

The strongest type of intermolecular force, specifically occurring in molecules containing hydrogen bonded to highly electronegative atoms like oxygen, nitrogen, or fluorine.

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How to Determine Molecular Polarity

The process of determining whether a molecule is polar or nonpolar, based on its molecular shape and the electronegativity difference of its atoms.

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Electronegativity

A measure of an atom's ability to attract electrons within a chemical bond. Greater the difference in electronegativity between atoms, stronger the polarity of the bond.

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Nonpolar Molecules

Molecules with zero net dipole moment due to their symmetrical shape and/or equal sharing of electrons.

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Polar Molecules

Molecules with asymmetric shapes and a net dipole moment due to unequal sharing of electrons.

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Boiling Point

The temperature at which a substance transitions from a liquid state to a gaseous state. Substances with stronger intermolecular forces (IMFs) have higher boiling points.

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Catalysts and Reaction Rate

Catalysts speed up reactions by providing an alternative pathway with lower activation energy.

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Catalysts and Equilibrium

Catalysts do not change the position of equilibrium or the equilibrium constant (K). They only speed up the rate at which equilibrium is reached.

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Catalysts and Enthalpy

Catalysts do not affect the enthalpy change (ΔH) of a reaction. They simply make the reaction faster.

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Activation Energy

The minimum energy required for a collision between molecules to result in a reaction.

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Collision Theory

Reactions occur when molecules collide with enough energy and in the correct orientation.

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Reduction

The process of a substance gaining electrons, resulting in a decrease in oxidation number.

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Oxidation

The process of a substance losing electrons, resulting in an increase in oxidation number.

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Redox Reaction

A chemical reaction involving both oxidation and reduction, where one substance is oxidized while another is reduced.

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Quantum Mechanical Model

A model of the atom that describes electrons as existing in probability clouds or orbitals, where their positions are uncertain. Unlike the Bohr model, it considers electrons as both waves and particles, using quantum numbers to describe their energy levels and positions.

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Heisenberg Uncertainty Principle

A principle that states that you cannot know both an electron's position and momentum exactly at the same time.

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VSEPR Theory

The arrangement of atoms in a molecule, determined by the repulsion between electron pairs in the valence shell.

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Exothermic Reaction

A chemical reaction that releases heat to the surroundings, and the equilibrium constant (K) decreases with increasing temperature.

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Endothermic Reaction

A chemical reaction that absorbs heat from the surroundings, and the equilibrium constant (K) increases with increasing temperature.

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Stress (in Equilibrium)

A change in reaction conditions (like temperature, pressure, or concentration) that shifts the equilibrium to relieve the stress and favor either reactants or products.

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Catalyst

A substance that speeds up a chemical reaction without being consumed in the process.

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Equilibrium Constant (K)

The ratio of products to reactants at equilibrium, representing the extent to which a reaction proceeds to completion.

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Study Notes

Organic Chemistry - Unit 1

  • Structural Isomers: Compounds with the same chemical formula but different structures. Example: Hexane and 2-Methylpentane.

Functional Groups

  • Alcohols: Contain a hydroxyl (-OH) group bonded to a carbon atom. Example: Ethanol (CH3CH2OH).
  • Aldehydes: Contain a carbonyl group (carbon double bonded to an oxygen) attached to a hydrogen and a carbon group.
  • Ketones: Contain a carbonyl group (carbon double bonded to an oxygen) attached to two carbon groups.
  • Carboxylic Acids: Contain a carboxyl (-COOH) group. Example: Acetic Acid (CH3COOH).
  • Esters: Contain a (-COO-) group between two carbon chains. Example: Ethyl Acetate (CH3COOCH2CH3).
  • Amines: Contain an amino (-NH2) group. Example: Methyl Amine (CH3NH2).
  • Amides: Contain a (-CONH2) group. Example: Acetamide (CH3CONH2).

Other Functional Groups

  • Alkenes: Two carbons with a double bond.
  • Alkynes: Two carbons with a triple bond.
  • Ethers: Contain an oxygen atom bonded to two carbon atoms.
  • Halides: Contain a halogen (F, Cl, Br, or I) bonded to a carbon.
  • Thiols: Contain a sulfur atom bonded to a hydrogen and a carbon.
  • Phenol: A hydroxyl group attached to an aromatic/benzene ring

Reactions in Organic Chemistry

  • Oxidation Reactions:
    • Primary alcohols become aldehydes during oxidation.
    • Secondary alcohols become ketones during oxidation.
    • Tertiary alcohols do not undergo oxidation.
    • Aldehydes become carboxylic acids during oxidation.
  • Addition Reactions: Alkenes and alkynes can react with other molecules under specific conditions like heat or light to add atoms or groups to them.
    • Hydrogenation: Adding hydrogen (H2).
    • Hydration: Adding water (H2O).
    • Halogenation: Adding halogens (Cl2 or Br2).
  • Substitution Reactions: Nucleophilic Substitution: A nucleophile (strong electron donor) attacks an alkyl halide replacing the halide. Electrophilic Substitution - The replacement of a hydrogen in the ring by an electrophile.

Summary Table of Functional Groups

Compound Type Functional Group Example Structure
Amines -NH2 Methylamine (CH3NH2) CH3-NH2
Amides -CONH2 Acetamide (CH3CONH2) CH3-C-NH2
Ketones C=O Acetone (CH3COCH3) CH3-C-CH3
Aromatics Benzene ring Benzene (C6H6) C6H6
Esters -COO- Ethyl Acetate (CH3COOCH2CH3) CH3-C-O-CH2CH3

Unit 2: Atomic Structure & Chemical Bonding

  • Electron Configurations (Neutral + Cation) for Copper and Chromium: Copper (Cu) [Ar] 4s1 3d10, Copper 2+ [Ar] 3d9, Chromium (Cr) [Ar] 4s1 3d5, Chromium 3+ [Ar] 3d3
  • Intermolecular Forces: London Dispersion, Dipole-Dipole, and Hydrogen bonds.
  • How to Identify Intermolecular Bonds:
    • Nonpolar molecules: Dispersion forces.
    • Polar molecules: Dispersion and dipole-dipole forces.
    • Molecules with O-H, N-H, or F-H bonds: Dispersion, dipole-dipole, and hydrogen bonding

Unit 3: Kinetics

  • Temperature effects on equilibrium: For exothermic reactions, raising temperature decreases the equilibrium constant (K). For endothermic reactions, raising temperature increases K.
  • Catalysts: Catalysts do not change the position of equilibrium or the equilibrium constant (K), they do not alter ΔH, they only speed up the reaction
  • Le Chatelier's principle: The system will shift equilibrium to minimize the stress or change exerted upon it. A change in concentration, temperature, or pressure of reactants or products will result in the movement of the equilibrium.

Unit 4: Acids and Bases

  • Redox reactions: Changes in oxidation numbers of elements, involving loss and gain of electrons.
  • No redox reaction: Oxidation numbers of all elements remain unchanged

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