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Inorganic Chemistry- Special Topics

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Transmetallation

Back (Answer)

M + M’R -> MR + M’, where M is a metal that is more electropositive than M’

#2
Front (Question)

Double displacement

Back (Answer)

MR + EX -> MX + ER, where E is a p-block element metalloid and M is more electropositive than E

#3
Front (Question)

Hydrometallation

Back (Answer)

MH + H2C=CH2 -> MH2C-CH3, in the case of unsymmetrical Allene’s, the M group attaches to the less hindered carbon atom, and the smaller H attaches to the most hindered C

#4
Front (Question)

S block elements form organometallic compounds that have what type of bonds?

Back (Answer)

Highly polar M+-C- bonds; the ionic character of these bonds increases for the heavier elements

#5
Front (Question)

Polarity of s-block organometallics vs group 3 organometallics

Back (Answer)

Group 3 organometallic compounds are more polar in nature

#6
Front (Question)

Group 3 nucleophilic character trend:

Back (Answer)

AlR3>GaR3>BR3; BR3 & GaR3 compounds are unassociated planar trigonal molecules

#7
Front (Question)

Group 4 organometallic polarity

Back (Answer)

Not very polar and organometallic compounds are electron-poor

#8
Front (Question)

Group 4 organometallic geometry

Back (Answer)

Tetrahedral

#9
Front (Question)

Group 4 organometallic resistance to hydrolysis

Back (Answer)

Resistance is due to low polarity of their bonds and the steric hinderance around the center atom

#10
Front (Question)

Group 5 organometallic geometry

Back (Answer)

Trigonal pyramidal

#11
Front (Question)

Group 5 organometallic compounds electron density

Back (Answer)

Electron rich; Lewis basicity arises due to the presence of a lone pair of e- on the center atom

#12
Front (Question)

Hapticity

Back (Answer)

The # of atoms of a ligand that are attached to a metal atom; ranges from 1-8

#13
Front (Question)

Group 6, 7, & 8 organometallic compounds generally have

Back (Answer)

18 valence electrons around their central metal atom

#14
Front (Question)

Toxic organometallic compounds

Back (Answer)

Organomercury, organoptin, organolead, organoarsenic, organosilicon

#15
Front (Question)

Biomethylation

Back (Answer)

Creation of organometallic compounds created in the environment starting from inorganic precursors

#16
Front (Question)

Catalyst

Back (Answer)

A substance that increases the rate of a chemical reaction without being consumed; they act by lowering the activation energy of rxns

#17
Front (Question)

Homogenous catalysis

Back (Answer)

The catalyst and reagents are present in the same phase

#18
Front (Question)

Heterogeneous catalysis

Back (Answer)

The catalyst is present in a phase different from that of the reactants; solids and are usually easily separated from the products of the rxns

#19
Front (Question)

Turnover frequency

Back (Answer)

N, the ratio of he rate of rxn (v) over the concentration of the catalyst [C] in a homogenous catalyst or the amount of catalyst in a heterogeneous catalyst

#20
Front (Question)

Four distinct characteristics of catalytic process

Back (Answer)

• ) must be thermodynamically favorable • ) fast enough to be useful • ) catalyst = selective and yield high proportion of desired product • ) have a long lifetime and not be altered over many rxns

#21
Front (Question)

Homogenous Catalytic process of hydrocarbon formation

Back (Answer)

• ) coordination and issociation of reactants and catalyst • ) migration • ) nuchleophilic attack • ) oxidation and reduction • ) oxidative addition

#22
Front (Question)

Materials chemistry

Back (Answer)

Solid state chemistry; the synthesis, structure, properties, and applications of solid materials

#23
Front (Question)

Defect structure

Back (Answer)

Aspect of solids that affect properties such as electrical conductivity, mechanical strength, corrosion, and chemical reactivity

#24
Front (Question)

Point defects

Back (Answer)

Occur at single sites; can be intrinsic or extrinsic