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AP Chemistry 4.7 Types of Chemical Reactions Study Notes

AP Chemistry 4.7 Types of Chemical Reactions Study Notes - New Syllabus Effective fall 2024

AP Chemistry 4.7 Types of Chemical Reactions Study Notes- New syllabus

AP Chemistry 4.7 Types of Chemical Reactions Study Notes – AP Chemistry –  per latest AP Chemistry Syllabus.

LEARNING OBJECTIVE

Identify a reaction as acid-base, oxidation-reduction, or precipitation.

Key Concepts: 

  • Identifying Acid-Base Reactions
  • Oxidation-Reduction Reactions
  • Assigning Oxidation Numbers
  • Oxidation-Reduction (Redox) Reactions
  • Precipitation Reactions

AP Chemistry-Concise Summary Notes- All Topics

4.7.A.1 Acid-Base Reactions: Proton Transfer:

1. Definition of Acids and Bases:

i. Arrhenius Definition:
Acid: A substance that increases the concentration of hydrogen ions (H⁺) or protons when dissolved in water.
Base: A substance that increases the concentration of hydroxide ions (OH⁻) when dissolved in water.
Example:
Acid: HCl → H⁺ + Cl⁻
Base: NaOH → Na⁺ + OH⁻

ii.Bronsted-Lowry Definition:
Acid: A proton (H⁺) donor.
Base: A proton (H⁺) acceptor.
Example:
In the reaction

HCl+H₂OCl+H₃O+\text{HCl} + \text{H₂O} \rightleftharpoons \text{Cl}⁻ + \text{H₃O}⁺

, HCl contributes a proton (an acid), and H₂O accepts a proton (a base).

iii. Lewis Definition:
Acid: A species that can accept a pair of electrons to form a coordinate covalent bond.
Base: A substance that can donate a pair of electrons to form a coordinate covalent bond.
Example: In the reaction between boron trifluoride (BF₃) and ammonia (NH₃), BF₃ acts as the Lewis acid (electron pair acceptor), and NH₃ acts as the Lewis base (electron pair donor).

2. Proton Transfer Mechanism:

The proton transfer mechanism is the basis of many acid-base reactions, especially in aqueous solutions, where a proton, H⁺, which is simply a hydrogen atom without its electron, moves from one species to another. This mechanism can be understood by the roles of donors and acceptors.

i. Understanding H⁺ Ion Transfer:

The H⁺ ion is simply a bare nucleus—a single proton—since the hydrogen ionized loses its lone electron. Thus, it’s very reactive and can readily bond with other species. In aqueous solution, the H⁺ ion does not appear often in its bare form but is instead often present as the hydronium ion, H₃O⁺, bonded to a water molecule.

The transfer of H⁺ is accompanied by breaking up the bonds in which the proton is withdrawn from one molecule-the acid-and forms a bond where the proton is accepted by another molecule-the base. The reaction can often be written in an equilibrium form as follows:

HAH++A\text{HA} \rightleftharpoons \text{H}^+ + \text{A}^-

In this, HA is a kind of acid, from whence the H⁺ ion has been removed, and A⁻ is a conjugate base.

ii. Role of Donors and Acceptors:

In the case of proton transfer, we class substances into two primary roles:

Proton Donor (Acid):
A proton donor is a substance that can release or donate a proton (H⁺) to another species.
The Bronsted-Lowry definition defines an acid as any substance that donates a proton in a reaction.
Example: In the dissociation of hydrochloric acid (HCl):

HClH++Cl\text{HCl} \rightarrow \text{H}^+ + \text{Cl}^-

Here, HCl is the proton donor.

Proton Acceptor (Base):
A proton acceptor is a species that can receive or accept a proton (H⁺) from another species.
As per the Bronsted-Lowry definition, a base is any species that accepts a proton in a reaction.
Example: Ammonia with water.

 

NH3+H2ONH4++OH\text{NH}_3 + \text{H}_2\text{O} \rightarrow \text{NH}_4^+ + \text{OH}^-

 

iii. Water as a Proton Transfer Species:
Water is both an acid and a base. The very small fraction of water molecules ionizes in pure water to form hydronium (H₃O⁺) and hydroxide ions (OH⁻):

H₂OH++OH

When H₂O acts as a proton donor, it forms OH⁻. Conversely, when it acts as

If H₂O acts as a proton donor, then it creates OH⁻, and if it acts as a proton acceptor, then it creates H₃O⁺.

In summary, proton transfer consists of the donation of a proton, H⁺, from acid to the base. Hence, it forms new bonds and shifts it around. The acid is the proton donor, and the base is the proton acceptor. The movement of the proton plays a crucial role in many chemical and biological processes, such as enzyme functions, acid-base control in the body, and acid-base reactions in aqueous solutions.

3. Conjugate Acid-Base Pairs:

A conjugate acid-base pair is two species that vary by one proton (H⁺).
Acid: loses a proton (H⁺).
Base: gains a proton (H⁺).
,When an acid releases a proton the species produced will be its conjugate base, and when a base accepts a proton, the species formed will be its conjugate acid.

Examples:
i. HCl (acid) → Cl⁻ (conjugate base)
ii. CH₃COOH (acid) → CH₃COO⁻ (conjugate base)
iii. NH₃ (base) → NH₄⁺ (conjugate acid)
iv. H₂O (acid) → OH⁻ (conjugate base)
v. H₂SO₄ (acid) → HSO₄⁻ (conjugate base)

Note: Strong acids have weak conjugate bases, and strong bases have weak conjugate acids.

4. Strength of Acids and Bases:

Strong Acids/Bases: Completely ionize in water.
Example: HCl (acid), NaOH (base).
Characteristics: High H⁺ or OH⁻ concentration, very low (acid) or high (base) pH.

Weak Acids/Bases: Partially ionize in water.
Example: CH₃COOH (acid), NH₃ (base).
Characteristics: Low H⁺ or OH⁻ concentration, moderate pH.

Ionization in Water:
The strong acids/bases fully ionize, whereas the weak acids/bases form an equilibrium state, almost completely ionizing.

5. pH and Buffers:

  • pH and pOH

i. Relationship between [H⁺] and pH:
pH measures the acidity of a solution based on the concentration of hydrogen ions [H⁺].
pH is calculated as:

pH=log[H+]\text{pH} = -\log[H⁺]

High [H⁺] = low pH (acidic solution).
Low [H⁺] = high pH (basic solution).

ii. Calculating pH and pOH:
pOH is a measure of the basicity of a solution in terms of the hydroxide ion concentration [OH⁻].
pOH is defined as:   pOH = -log[OH⁻]
Relationship:

pH+pOH=14\text{pH} + \text{pOH} = 14

(In pure water at 25°C,

[H+]=[OH]=1×107[H⁺] = [OH⁻] = 1 \times 10^{-7}

, so pH = 7 and pOH = 7).
Neutralization occurs when an acid reacts with a base to form water and a salt.

  • Buffers and Buffering Capacity

Importance of Buffers to Maintain pH**
Buffer solutions resists a drastic change in their pH when acid or base solution is added little by little in small quantities
buffers are, therefore, importance in biological tissues such as that in bloods, which makes sure that life continues with good performance
How Buffers Function in Acids and bases:
Buffered solution is, therefore, weak acid-salt of this weak acid /weak base/ salt of a weak base.
When an acid is added, the buffer absorbs the H⁺ ions, and when a base is added, the buffer releases H⁺ ions to maintain pH.
Example: In blood, the carbonic acid (H₂CO₃) and bicarbonate (HCO₃⁻) buffer system helps maintain a pH of about 7.4.

Buffers effectively neutralize added acids or bases by shifting equilibrium to maintain constant pH.

4.7.A.2 Oxidation-Reduction (Redox) Reactions and Combustion:

1. Basic Concepts of Redox Reactions:

i. Oxidation and Reduction:
Oxidation: Loss of electrons; increases oxidation number.

ii. Reduction: Gain of electrons; decreases oxidation number.

 Both happen together in a redox reaction.

iii. Oxidation Number:
The imaginary charge of an atom according to electron transfer rules.
Examples: In H₂O, oxygen is -2, and hydrogen is +1.

iv. Electron Transfer:
Electrons move from the oxidized species (loses electrons) to the reduced species (gains electrons).
Example: Zn → Zn²⁺ + 2e⁻ (oxidized) and Cu²⁺ + 2e⁻ → Cu (reduced).

2. Combustion Reactions:

Combustion Reactions:
i. Complete Combustion:
Hydrocarbons react with oxygen to produce carbon dioxide (CO₂) and water (H₂O).
Example: CH₄ + 2O₂ → CO₂ + 2H₂O

Incomplete Combustion:
Limited oxygen results in the formation of carbon monoxide (CO) and/or soot (C), along with CO₂ and H₂O.
Example: 2CH₄ + 3O₂ → 2CO + 4H₂O (incomplete combustion)

Oxidation States in Combustion:
In complete combustion, carbon in the hydrocarbon is oxidized from an oxidation state of -4 (in methane, CH₄) to +4 (in CO₂).
In incomplete combustion, carbon may be partially oxidized to form CO, where its oxidation state is +2, or remain as elemental carbon (oxidation state 0).

The oxidation state is tracked to determine the changes of elements, especially carbon and oxygen, during combustion reactions.

3. Energy Changes in Redox and Combustion Reactions:

  • Exothermic Nature:
    Combustion reactions are exothermic. This means energy is released from combustion in the form of heat and light.
    During the process of combustion, chemical bonds break and form new bonds; it is highly exothermic as more energy is released compared to the consumed amount.
  • Heat of Combustion:
    The heat of combustion is the energy given out when a substance undergoes complete combustion with oxygen.
    The usual unit for growth of energy is kJ/mol, and so it determines how much energy is generated when a given amount of fuel burns.
    For example, the combustion of methane, CH₄, releases a lot of energy to be used in heating or in electricity production.

4.7.A.3 Redox Reactions: Electron Transfer:

1. Definition of Oxidation and Reductioni

                   i. Oxidation:

    • Oxidation is the process where a substance loses electrons. As a result, the oxidation state of the atom or ion increases.
    • Example: In the reaction of magnesium with oxygen (Mg + O₂ → MgO), magnesium loses two electrons, going from 0 to +2 oxidation state.

      ii . Reduction:

      • Reduction is the process where a substance gains electrons. This causes the oxidation state of the atom or ion to decrease.
      • Example: In the same reaction (Mg + O₂ → MgO), oxygen gains electrons, going from 0 to -2 oxidation state.

In a redox (reduction-oxidation) reaction, oxidation and reduction always happen together. One substance is oxidized (loses electrons), and another is reduced (gains electrons).

2. Electron Transfer in Redox Reactions:

  • Oxidation involves the loss of electrons. The species that loses electrons becomes oxidized.
  • Reduction involves the gain of electrons. The species that gains electrons becomes reduced.

In a redox reaction, the electrons that are lost during oxidation are transferred to another species, which gains them during reduction. This transfer of electrons is what drives the entire redox process.

For example, in the reaction between hydrogen and oxygen to form water:     

2H2+O22H2O2H_2 + O_2 \rightarrow 2H_2O

  • Oxidation: Hydrogen (H) loses electrons, going from an oxidation state of 0 to +1 (H₂ → 2H⁺ + 2e⁻).
  • Reduction: Oxygen (O) gains electrons, going from an oxidation state of 0 to -2 (O₂ + 4e⁻ → 2O²⁻).

The electrons lost by hydrogen are transferred to oxygen, allowing the formation of water. The electron transfer is what balances the overall reaction and completes the redox process.

4.7.A.4 Using Oxidation Numbers to Identify Oxidized and Reduced Species:

1. Rules for Assigning Oxidation Numbers:

i. Element in its pure form: The oxidation number is 0 (e.g., O₂, N₂, H₂).
ii. Monatomic ions: The oxidation number is equal to the charge of the ion (e.g., Na⁺ = +1, Cl⁻ = -1).
iii. Oxygen: Usually -2 in compounds (except in peroxides, where it’s -1, or with fluorine).
iv. Hydrogen: Usually +1 when bonded to nonmetals, and -1 when bonded to metals.
v. Fluorine: Always -1 in compounds.
vi. Sum of oxidation numbers: The sum of oxidation numbers in a neutral compound is 0, and in a polyatomic ion, it is equal to the charge of the ion.
7. Group 1 metals: Always +1 in compounds.
8. Group 2 metals: Always +2 in compounds.

2. Tracking Oxidation Number Changes:

i. Identify oxidation numbers: Assign oxidation numbers for all elements in both the reactants and products according to the rules.

ii. Compare oxidation numbers:
Oxidation: If the oxidation number of an element increases (an increase is a net loss of electrons), that element is oxidized.

Reduction: If the oxidation number of an element decreases (a decrease is a net gain of electrons), that element is reduced.

iii. Track the electron flow: In a redox reaction, electrons are transferred from the oxidized species to the reduced species.

iv. Balance changes in oxidation numbers: Check that the total increase in oxidation numbers equals the total decrease, indicating that the process is a balanced transfer of electrons.

Example:

In the reaction: –
Zn + CuSO₄ → ZnSO₄ + Cu
Zn goes from 0 to +2 (oxidized).
Cu²⁺ goes from +2 to 0 (reduced).

This indicates the transfer of electrons from zinc to copper.

4.7.A.5 Precipitation Reactions and Solubility Rules

1. Definition of Precipitation Reactions:

A precipitation reaction is a reaction in which two soluble substances react in solution to form an insoluble product, called a precipitate. The precipitate forms because it has low solubility in the solvent (usually water) and separates from the solution.

Example:
When silver nitrate (AgNO₃) reacts with sodium chloride (NaCl), the insoluble precipitate silver chloride (AgCl) forms: AgNO₃ (aq)+NaCl (aq)→AgCl (s)+NaNO₃ (aq)

Here, AgCl is the precipitate.

2. Solubility of Common Salts: The solubility of salts in water depends on their chemical properties. Here are some general rules for common salts:
i. Most Group 1 salts (alkali metal salts) are soluble:
Example: Sodium chloride (NaCl), Potassium sulfate (K₂SO₄).

ii. Most nitrate salts (NO₃⁻) are soluble:
Example: Potassium nitrate (KNO₃), Calcium nitrate (Ca(NO₃)₂).

iii. Most ammonium salts (NH₄⁺) are soluble:
Example: NH₄Cl.

iv. Most chloride salts (Cl⁻) are soluble, except for those of silver (Ag⁺), lead (Pb²⁺), and mercury (Hg²⁺):
Example: NaCl is soluble, but AgCl is insoluble.

v. Most sulfate salts (SO₄²⁻) are soluble, except for those of barium (Ba²⁺), calcium (Ca²⁺), and lead (Pb²⁺):
Example: Na₂SO₄ is soluble, but BaSO₄ is insoluble.

vi. Most carbonate (CO₃²⁻) and phosphate (PO₄³⁻) salts are insoluble, except for those of Group 1 metals and ammonium:
Example: Sodium carbonate (Na₂CO₃) is soluble, but calcium carbonate (CaCO₃) is insoluble.

These solubility rules help predict the formation of precipitates in reactions involving salts.

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