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Comprehensive practice flashcards covering vocabulary, reactions, and nomenclature for the JEE Haloalkanes and Haloarenes chapter.
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Haloalkane (Alkyl halide)
A compound formed by the replacement of hydrogen atom(s) in an aliphatic hydrocarbon by halogen atom(s), where the halogen is attached to an sp3 hybridised carbon atom.
Haloarene (Aryl halide)
A compound formed by the replacement of hydrogen atom(s) in an aromatic hydrocarbon by halogen atom(s), where the halogen is attached to an sp2 hybridised carbon atom of an aryl group.
Geminal-dihalides
Dihalides where two halogen atoms are attached to the same carbon atom; their common name is Alkylidene halides (e.g., Ethylidene chloride).
Vicinal dihalides
Dihalides where two halogen atoms are attached to adjacent carbon atoms; their common name is Alkylene dihalides (e.g., Ethylene dibromide).
Allylic halides
Compounds in which the halogen atom is bonded to an sp3-hybridised carbon atom situated next to a carbon-carbon double bond (C=C).
Benzylic halides
Compounds in which the halogen atom is bonded to an sp3-hybridised carbon atom situated next to an aromatic ring.
Vinylic halides
Compounds in which the halogen atom is bonded to an sp2-hybridised carbon atom of a carbon-carbon double bond.
Bond Enthalpy Order
The order of bond energy for methyl halides is H3C−F>H3C−Cl>H3C−Br>H3C−I.
Bond Length Order
The order of distance between the carbon and halogen atoms is H3C−F<H3C−Cl<H3C−Br<H3C−I.
Dipole Moment Exception
In the dipole moment order for methyl halides, chloromethane precedes fluoromethane: H3C−Cl>H3C−F>H3C−Br>H3C−I.
Lucas Reagent
A mixture of concentrated HCl and anhydrous ZnCl2 used to distinguish between 1∘,2∘, and 3∘ alcohols.
Darzen's Process
The reaction of alcohols with Thionyl Chloride (SOCl2) to prepare pure alkyl halides, as the gaseous by-products (SO2 and HCl) escape the reaction mixture.
Kharash Effect (Peroxide Effect)
The addition of HBr to unsymmetrical alkenes in the presence of peroxides, resulting in the major product following Anti-M Rule (Anti-Markovnikov addition).
NBS (N-Bromo succinimide)
A reagent used specifically for substitution at allylic and benzylic positions using a free radical mechanism.
Test for Unsaturation
The decolourisation of a Bromine (Br2) solution in CCl4 when it reacts with an alkene or alkyne.
Finkelstein Reaction
A halogen exchange reaction where alkyl chlorides or bromides react with NaI in dry acetone to form alkyl iodides (R−I).
Swarts Reaction
A halogen exchange reaction used to synthesize alkyl fluorides (R−F) using metallic fluorides such as AgF,Hg2F2,SbF3, or CoF2.
Gattermann Reaction
The preparation of aryl halides by treating benzene diazonium salts with HCl or HBr in the presence of copper powder.
Sandmeyer Reaction
The preparation of aryl halides using benzene diazonium chloride and cuprous halides (Cu2Cl2 or Cu2Br2).
Hunsdiecker Reaction
The preparation of alkyl bromides by reacting silver salts of carboxylic acids (R−COOAg) with Br2 in CCl4 via free radical mechanism.
Walden Inversion
The 100% inversion of configuration that occurs during an SN2 (Substitution nucleophilic Bimolecular) reaction.
Ambident Nucleophiles
Nucleophiles that possess two donor sites but use only one at a time to form a bond (e.g., CN−,NO2−,SCN−).
Saytzeff Rule
In elimination reactions, the most stable alkene (the more substituted one with more α-hydrogens) is the major product.
Grignard Reagent
Organometallic compounds formed by the reaction of alkyl halides with Magnesium in dry ether, represented by the general formula R−MgX.
Wurtz Reaction
The coupling of two alkyl halides with Sodium in dry ether to form a symmetrical hydrocarbon (R−R).
Fittig Reaction
The reaction of two aryl halides with Sodium in dry ether to form Biphenyl.
Phosgene
A toxic, extremely poisonous gas (COCl2) formed by the slow oxidation of chloroform (CHCl3) by air in the presence of sunlight.
DDT
p,p'-Dichlorodiphenyltrichloroethane; a polyhalogen compound effectively used against mosquitoes that spread malaria.
Chloropicrin (Tear gas)
A compound with the formula CCl3NO2, synthesized by reacting Chloroform with concentrated nitric acid (HNO3).
Freons
Chlorofluorocarbon compounds of methane and ethane that are extremely stable, non-toxic, noncorrosive, and used in refrigeration.