AP Chemistry Unit 4

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35 Terms

1
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Dissolution as both a physical and chemical change

Dissolving NaCl in water is physical due to the identity of Na⁺ and Cl⁻ remaining the same, but it involves breaking ionic bonds and forming ion-dipole interactions, suggesting a chemical component.

2
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Evidence of chemical change from precipitation

The formation of a precipitate indicates a new substance with different solubility was created, demonstrating that composition has changed.

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Phase change and composition

In boiling water, molecules remain H₂O despite changes in spacing and intermolecular forces, indicating only a physical change.

4
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Heat as evidence for change

Heat production alone cannot confirm a chemical reaction; the presence of gas evolution or other changes indicates a chemical change.

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Melting ice vs. combustion of methane

Melting ice is a physical change with no new substances formed; combustion of methane is a chemical change generating CO₂ and H₂O.

6
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Molecular equation for precipitation

The molecular equation for CaCl₂(aq) + Na₂CO₃(aq) indicates the formation of CaCO₃(s) as a precipitate.

7
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Complete ionic equation components

The complete ionic equation includes all ions present, while net ionic eliminates spectator ions to show actual reaction components.

8
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Checking a net ionic equation

To validate a net ionic equation, ensure strong electrolytes are represented as ions, confirm charge and atom balance, and check for species undergoing chemical changes.

9
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Usage of molecular and complete ionic equations

Molecular equations are used for overall processes, complete ionic for showing dissociation of strong electrolytes, and net ionic focuses on reacting species.

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Conditions for 'no net ionic equation'

If all reactants and products remain in aqueous form with no precipitate, gas, or weak electrolyte formation, there is no net ionic equation.

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Particulate model for Mg + HCl reaction

In the reaction of Mg with HCl, electrons transfer to form Mg²⁺ and H₂ gas, with spectator ions remaining in solution.

12
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Converting balanced equations to particulate models

Each coefficient in a balanced equation corresponds to the specific quantity of molecules or ions represented in a particulate model.

13
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Strong vs. weak electrolytes

Strong electrolytes fully dissociate in solution, while weak electrolytes only partially dissociate, affecting their conductivity.

14
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Physical vs. chemical change in particulate models

Physical changes retain the same molecular identity but alter spacing; chemical changes rearrange atoms and bonds to create different substances.

15
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Limiting reactant identification in models

The limiting reactant is completely consumed first, reflected in its absence in the product representation, while excess reactant remains.

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Vaporization vs. decomposition energy requirements

Vaporization requires less energy than decomposition because only intermolecular forces are broken in vaporization.

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Dissolving LiBr characterization

Dissolving LiBr involves breaking ionic bonds but retains the identity of Li⁺ and Br⁻ as solvated ions.

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Bond changes in H₂ + O₂ reaction

The reaction of H₂ and O₂ involves breaking bonds that requires energy, while new bonds formed release energy, indicating an exothermic process.

19
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Heat curve plateaus explanation

Plateaus in heating curves represent states of phase change where the temperature remains constant while energy disrupts intermolecular forces.

20
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Candle burning as simultaneous processes

The process of burning a candle exhibits both physical (melting) and chemical changes (combustion of hydrocarbons).

21
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Stoichiometry in reacting substances

Through stoichiometry, the balance of reactants and products is determined by analyzing their molar ratios and limiting reactants.

22
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Coefficients and subscripts differentiation

Coefficients indicate the number of molecules in a reaction; subscripts indicate the number of atoms within each molecule.

23
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Possible reasons for less than 100% yield

Reasons for yield below 100% include side reactions, incomplete reactions, and product loss during transfer.

24
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Linking stoichiometry with ideal gas law

Stoichiometric calculations can use PV = nRT to determine moles of a gas produced in a reaction.

25
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Using molarity in solutions stoichiometry

Molarity allows for conversion of volumes of solutions into moles for stoichiometric calculations.

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Difference in equivalence point and endpoint

Equivalence point occurs when moles of titrant equal moles of analyte, whereas the endpoint is indicated by a visual change.

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Calculating monoprotic acid concentration

To find concentration of a monoprotic acid, titrate against a strong base and use the relationship between molarity and volume.

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Effect of overshooting endpoint in titrations

Overshooting the titration endpoint leads to an inaccurately low calculated concentration for the acid.

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Titration curve differences between strong and weak acids

Strong acid titrations have steep curves, while weak acids exhibit buffer regions and higher pH at equivalence due to ionization.

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Need for reactions to go to completion in titrations

Accurate titration results require complete reactions to ensure that titrant reflects true analyte amounts.

31
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Redox reaction details of Zn + CuSO₄

In this reaction, Zn is oxidized and Cu²⁺ is reduced; electrons transfer from Zn to Cu²⁺.

32
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Simultaneity of oxidation and reduction

Redox reactions must occur simultaneously as electrons cannot exist freely in solutions; oxidation must accompany reduction.

33
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Oxidation number assignment methodology

Assign oxidation numbers systematically based on elemental forms and charge rules to track electron transfer.

34
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Oxidation number changes comparison in reactions

In combustion, carbon is typically oxidized while in single displacement, metals oxidize, and ions are reduced.

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Oxidation numbers tracking electron flow

Oxidation numbers help identify which atoms lose or gain electrons during chemical reactions, thus revealing electron flow.

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