Haloalkanes and Haloarenes Practice Flashcards

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Comprehensive practice flashcards covering vocabulary, reactions, and nomenclature for the JEE Haloalkanes and Haloarenes chapter.

Last updated 10:19 AM on 6/10/26
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30 Terms

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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 sp3sp^3 hybridised carbon atom.

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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 sp2sp^2 hybridised carbon atom of an aryl group.

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Geminal-dihalides

Dihalides where two halogen atoms are attached to the same carbon atom; their common name is Alkylidene halides (e.g., Ethylidene chloride).

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Vicinal dihalides

Dihalides where two halogen atoms are attached to adjacent carbon atoms; their common name is Alkylene dihalides (e.g., Ethylene dibromide).

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Allylic halides

Compounds in which the halogen atom is bonded to an sp3sp^3-hybridised carbon atom situated next to a carbon-carbon double bond (C=CC=C).

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Benzylic halides

Compounds in which the halogen atom is bonded to an sp3sp^3-hybridised carbon atom situated next to an aromatic ring.

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Vinylic halides

Compounds in which the halogen atom is bonded to an sp2sp^2-hybridised carbon atom of a carbon-carbon double bond.

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Bond Enthalpy Order

The order of bond energy for methyl halides is H3CF>H3CCl>H3CBr>H3CIH_3C-F > H_3C-Cl > H_3C-Br > H_3C-I.

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Bond Length Order

The order of distance between the carbon and halogen atoms is H3CF<H3CCl<H3CBr<H3CIH_3C-F < H_3C-Cl < H_3C-Br < H_3C-I.

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Dipole Moment Exception

In the dipole moment order for methyl halides, chloromethane precedes fluoromethane: H3CCl>H3CF>H3CBr>H3CIH_3C-Cl > H_3C-F > H_3C-Br > H_3C-I.

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Lucas Reagent

A mixture of concentrated HClHCl and anhydrous ZnCl2ZnCl_2 used to distinguish between 1,2,1^\circ, 2^\circ, and 33^\circ alcohols.

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Darzen's Process

The reaction of alcohols with Thionyl Chloride (SOCl2SOCl_2) to prepare pure alkyl halides, as the gaseous by-products (SO2SO_2 and HClHCl) escape the reaction mixture.

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Kharash Effect (Peroxide Effect)

The addition of HBrHBr to unsymmetrical alkenes in the presence of peroxides, resulting in the major product following Anti-M Rule (Anti-Markovnikov addition).

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NBS (N-Bromo succinimide)

A reagent used specifically for substitution at allylic and benzylic positions using a free radical mechanism.

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Test for Unsaturation

The decolourisation of a Bromine (Br2Br_2) solution in CCl4CCl_4 when it reacts with an alkene or alkyne.

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Finkelstein Reaction

A halogen exchange reaction where alkyl chlorides or bromides react with NaINaI in dry acetone to form alkyl iodides (RIR-I).

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Swarts Reaction

A halogen exchange reaction used to synthesize alkyl fluorides (RFR-F) using metallic fluorides such as AgF,Hg2F2,SbF3,AgF, Hg_2F_2, SbF_3, or CoF2CoF_2.

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Gattermann Reaction

The preparation of aryl halides by treating benzene diazonium salts with HClHCl or HBrHBr in the presence of copper powder.

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Sandmeyer Reaction

The preparation of aryl halides using benzene diazonium chloride and cuprous halides (Cu2Cl2Cu_2Cl_2 or Cu2Br2Cu_2Br_2).

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Hunsdiecker Reaction

The preparation of alkyl bromides by reacting silver salts of carboxylic acids (RCOOAgR-COOAg) with Br2Br_2 in CCl4CCl_4 via free radical mechanism.

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Walden Inversion

The 100% inversion of configuration that occurs during an SN2S_N2 (Substitution nucleophilic Bimolecular) reaction.

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Ambident Nucleophiles

Nucleophiles that possess two donor sites but use only one at a time to form a bond (e.g., CN,NO2,SCNCN^-, NO_2^-, SCN^-).

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Saytzeff Rule

In elimination reactions, the most stable alkene (the more substituted one with more α\alpha-hydrogens) is the major product.

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Grignard Reagent

Organometallic compounds formed by the reaction of alkyl halides with Magnesium in dry ether, represented by the general formula RMgXR-MgX.

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Wurtz Reaction

The coupling of two alkyl halides with Sodium in dry ether to form a symmetrical hydrocarbon (RRR-R).

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Fittig Reaction

The reaction of two aryl halides with Sodium in dry ether to form Biphenyl.

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Phosgene

A toxic, extremely poisonous gas (COCl2COCl_2) formed by the slow oxidation of chloroform (CHCl3CHCl_3) by air in the presence of sunlight.

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DDT

p,p'-Dichlorodiphenyltrichloroethane; a polyhalogen compound effectively used against mosquitoes that spread malaria.

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Chloropicrin (Tear gas)

A compound with the formula CCl3NO2CCl_3NO_2, synthesized by reacting Chloroform with concentrated nitric acid (HNO3HNO_3).

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Freons

Chlorofluorocarbon compounds of methane and ethane that are extremely stable, non-toxic, noncorrosive, and used in refrigeration.