Inorganic Chemistry Exam 1, Chapters 1 and 2 – Flashcards
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            S block elements
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        Colorless ions Silvery colored when neutral Important biological functions
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            F block elements
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        Mostly have 3+ charges Pale colored in solution No important biological functions
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            D block elements
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        Usually 2+ or 3+ charges Intermediate color intensity in solution Most have positive biological functions as ions or complexes
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            P block elements
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        Contains cations and anions Colorless in solution
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            Covalent radius
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        1/2 the internuclear distance 1/2 the length of the covalent bond  For a bond between 2 identical atoms
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            Ionic radii of cations/anions
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        The sums of the ionic radii
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            Van der waals radius
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        1/2 the internuclear distance to the nearest Cl nucleus in the next molecule
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            Sizes of radii
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        Cationic < covalent < anionic = van der waals Difference of 60pm between each type
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            Horizontal trend of atomic radii
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        Decrease moving from L to R More protons pull electrons closer, causing a smaller radius
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            Vertical trend of atomic radii
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        Increase from top to bottom
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            Scandide contraction
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        Nonexpansion in period 4 Involves Al and Ga
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            Lanthanide contraction
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        Nonexpansion in period 6
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            Bronsted-Lowry acid
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        Proton donor (becomes conj base)
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            Bronsted-Lowry base
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        Proton acceptor (becomes conj acid)
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            Amphiprotic
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        Something that is both basic and acidic, but not strongly either
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            6 strong acids
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        1. HCl 2. HBr 3. HI 4. H2SO4 5. HClO4 6. HNO3
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            Lower pKa
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        Lower pH = MORE ACIDIC
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            Lower pKb
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        Higher pH = MORE BASIC
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            Strong acids produce?
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        A weak conjugate base
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            Weak acids produce?
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        A strong conjugate base
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            Nonacidic cations
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        pKa > 14 Do not alter pH of solution
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            Feebly acidic cations
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        pKa between 11.5 and 14
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            Weakly acidic cations
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        pKa between 6 and 11.5
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            Moderately acidic cations
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        pKa between 1 and 6
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            Strongly acidic cations
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        pKa between -4 and 1 React violently and exothermically
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            Very strongly acidic cations
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        pKa < -4 Cannot actually exist in solution
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            Acidity of a metal cation solution depends on?
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        1. charge 2. radius 3. electronegativity
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            Charge and acidity of metal cations
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        As charge increases, acidity strongly increases due to increased interaction and more dissociation
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            Radius and acidity of metal cations
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        As radius increases, acidity decreases Increased stability of cation leads to less interactions
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            Electronegativity and acidity of metal cations
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        As electronegativity increases, acidity increases
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            Hydration enthalpies of cations are affected by?
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        1. charge 2. radius 3. electronegativity
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            Charge and hydration enthalpies of cations
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        As charge increases, deltaH gets more negative, acidity increases  Charge has the biggest effect on deltaH!!!!!!!!!
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            Radius and hydration enthalpies of metal cations
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        As radius increases, deltaH gets less negative, acidity decreases`
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            Electronegativity and hydration enthalpies of metal cations
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        As electronegativity increases, deltaH gets more negative and acidity increases
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            Maximum coordination number
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        The max number of atoms bound to the central atom Depends on the size of the atoms bound to the central atom Generally increases moving down the periodic table
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            Maximum coordination number for period 2
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        4
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            Maximum coordination number for periods 3 and 4
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        6
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            Maximum coordination number for periods 5 and 6
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        > 6, usually 8
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            When maximum coordination number is met?
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        No reaction will occur in water due to steric hindrance
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            Why do some elements have lower than normal coordination numbers?
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        Ions in periods 5 and 6 (Ag+, Sn3+, Hg+, Au+) attach as few as 2 water molecules The polarizing power of the cationic charge is concentrated on fewer water molecules Each water molecule is more polarized, leading to HIGHER THAN EXPECTED ACIDITY.
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            Henderson-Hasselbach equation
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        pH = pKa + log [conj base]/[conj acid]
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            Equivalence point
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        When moles of acid = moles of base In titration NOT IMPORTANT
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            Half-equivalence point
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        When concentrations of acid and base are equal pH at this point = pH at right boundary = pKa1
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            Predominance diagram
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        Anions on R Cations on L
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            Predominance diagrams and predicting reactions
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        If there is no overlap, the reactants cannot coexist as predominant forms in the same pH, so a reaction will occur (proton transferred L to R)  If there is overlap, the reactants can coexist so there will be NO REACTION
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            Nomenclature of group 16 hydrides
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        H2S: hydrogen sulfide H2Se: hydrogen selenide H2Te: hydrogen telluride
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            Nomenclature of group 14 hydrides
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        End in "-ane" Plumbane, stannane, germane, silane  Formulas written w/ H+ last to show that they are not predominantly acidic
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            Nomenclature of group 15 hydrides
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        End in "-ine" Bismuthine, arsine, phosphine  Formulas written with H+ last to show that they are not predominantly acidic
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            Nomenclature of group 17: hydrogen halides
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        In solution, they undergo acid dissociation and are named as hydrohalic acids
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            Predominance diagram of a nonacidic cation
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        Cation is predominant at all pH values
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            Predominance diagram of a feebly acidic cation
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        Precipitates hydroxides from 1M solutions at pH > 11.5-14
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            Predominance diagram of a weakly acidic cation
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        Precipitates metal hydroxides at pH 6-11.5 (neutral to slightly basic
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            Predominance diagram of a moderately acidic cation
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        Cation is predominant in solution at pH 1-6, ppt forms if the solution is not kept acidic
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            Predominance diagram of a strongly acidic cation
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        Cation is predominant in solution at pH -4 to 1 At most practical pH values there is a metal hydroxide ppt
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            Predominance diagram of a very strongly acidic cation
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        Cannot exist in water because it is impossible to have a pH that low in water
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            As concentration decreases?
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        The range of soluble species increases!!!
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            Hydrated anions
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        A H bond forms between a H on the water and the metal anion, ripping the H off the water molecule and producing OH- to form a basic solution
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            Nonbasic anions
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        pKb > 14 No detectable basicity Cl-, Br-, I- No tendency to combine with H+ ions in solution So much less basic than water that they cannot compete with water for H+ ions
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            Feebly basic anions
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        pKb values 11.5-14 No examples
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            Weakly basic anions
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        pKb values 6-11.5 Includes F-
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            Moderately basic anions
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        pKb values 1-6 Te2-
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            Strongly basic anions
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        pKb values -4 to 1 Se2-, S2-
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            Very strongly basic anions
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        pKb < -4 React irreversibly with water  O2- + H2O = 2OH-
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            Factors that affect basicity of anions
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        1. charge 2. radius
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            Charge and basicity of anions
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        As the charge gets larger and more negative, the basicity increases  Basicity increases moving L to R across a period
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            Radius and basicity of anions
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        As radius increases, basicity decreases  Basicity decreases moving down a group
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            Periodic trends in basicity
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        The further up and into the periodic table an element is, the more reactive its ion is (as long as charge is increasing)
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            Reactions between strong acids and bases
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        React to give species with overlapping ranges closer to the center of the predominance diagram
