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condition of complete combustion of alkanes
excess O2 + heat/ignition
catalyst of halogenation of alkanes
UV light or heat
condition of incomplete combustion of alkanes
limited O2 + heat/ignition
catalyst of incomplete combustion of alkanes
limited O2 + heat/ignition
catalyst of hydrogenation of alkenes
Pt/Pd/Ni
catalyst of hydrohalogenation of alkenes
no catalyst needed
catalyst of hydration of alkenes to alcohols
trace acid catalyst (H⁺)
catalyst of hydration of an alkyne
Acid catalyst
catalyst of full hydrogenation of alkynes to alkanes
Pt/Pd/Ni/Rh
catalyst of partial hydrogenation of alkynes to cis-alkenes
Lindlar catalyst
catalyst of hydrohalogenation of alkynes
no catalyst needed
catalyst of halogenation of alkynes
no catalyst needed
catalyst of electrophilic aromatic substitution of benzenes
Lewis acid (AlCl3 or FeCl3)
catalyst of halogenation of benzenes
Fe or FeX₃
catalyst of nitration of benzenes
H₂SO₄
catalyst of sulfonation of benzenes
Concentrated H₂SO₄
the catalyst of friedel-crafts alkylation of benzenes
AlCl₃ or FeCl₃
catalyst of friedel-crafts acylation of benzenes
AlCl₃ or FeCl₃
the catalyst of dehydration of alcohols to alkenes
Heat + strong acid
the catalyst of the oxidation of a primary alcohol to an aldehyde
PCC
catalyst of the oxidation of a primary alcohol to a carboxylic acid
Jones reagent or KMnO₄
catalyst of the oxidation of a secondary alcohol
any oxidizing agent
catalyst of the condensation of 2 alcohol molecules into an ether (acid catalyzed condensation of alcohols)
Heat + strong acid
catalyst of the addition of alcohol to alkenes (ether formation)
Acid catalyst
catalyst of the formation of ethylene oxide (epoxide)
Ag catalyst + heat + pressure
catalyst of a williamson (unsymmetric)ether synthesis (reaction of alkoxide with an alkyl halide)
no catalyst needed
the catalyst of peroxyacid epoxidation of an alkene into an epoxide and acid
no catalyst needed
catalyst of ring opening reactions of epoxides into alcohols
acidic/basic conditions
catalyst of the oxidation of aldehydes into carboxylic acids
any oxidizing agent
catalyst of the hydrogenation of aldehydes/ketones into alcohol
Pt/Pd/Ni
the catalyst of the addition of an alcohol to an aldehyde/ketone (Hemiacetal/hemiketal and acetal/ketal formation)
H+
catalyst of the addition of an alcohol to a carboxylic acid to produce an ester and water (Fischer esterification)
strong acid catalyst
catalyst of the acid hydrolysis of esters to produce a carboxylic acid and alcohol
acid + heat
catalyst of the base hydrolysis of esters (saponification) to produce a carboxylic acid anion (acid salt) and alcohol
base + heat
catalyst of ether reduction into primary alcohols
LiAlH₄
which is NOT a catalyst of the reduction of nitro compounds to prepare amines
NaCl, LiH
Which is a catalyst of the reduction of amides to amines
LiAlH4, ether
catalyst of reducing nitriles into amides
reducing agent
compounds of group 1A ions
soluble
the ammonium ion NH4+
soluble
all common nitrates (NO3-)
soluble
all common acetates (C2H3O2-)
soluble
most perchlorates (ClO4-)
soluble
all common chlorides (Cl-), bromides (Br-), and iodides (I-) except those of Ag+, Pb2+, and Hg2+
soluble
all common sulfates (SO2-), except those of Ca2+, Sr2+, Ba2+, Pb2+, and Ag+
soluble
all metal hydroxides (OH-), except those of group 1A, NH4+, and Ca2+, Sr2+, and Ba2+
insoluble
all sulfides (S2-), except group 1A, NH4+, Ca2+, Sr2+, and Ba2+
insoluble
all carbonates (CO32-) and phosphates (PO43-), except group 1A and NH4+
insoluble
the reduction of a benzenes carbonyl group using zinc amalgam
clemmensen reduction
the oxidation of alkylbenzenes using sulfuric acid produces
benzoic acids
how many OR and OH groups do hemiacetals/ketals have
1 OH and 1 OR