Genius Jnr - Use the following information to answer the next question. The chlorofluorocarbon compounds of and are collectively called freons. The information in which alternative completes the given statement?

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Use the following information to answer the next question.

The chlorofluorocarbon compounds of and are collectively called freons.

The information in which alternative completes the given statement?

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Produce Butan 2 Ol Reaction Ch3mgbr Result Addition Hbr 1 Phenyl Propene Reaction Alkyl Chlorides Bromides Sodium Iodide Dry Acetone Form Alkyl Iodide Known Following Compounds Highest Boiling Point Following Halides Undergoes Sn2 Reaction Faster Use Following Information Answer Next Question Correct Order Increasing Reactivity Given Compounds S Following Alternatives Use Dichloromethane Following Polyhalogen Compounds Used Antiseptic Use Following Information Answer Next Question Chlorofluorocarbon Compounds Collectively Called Freo Phosgene Common Name Use Following Information Answer Next Question Information Alternative Completes Given Equation Following Alkyl Halides Produced Swarts Reaction Correct Order Increasing Density N Propyl Halides Structure Iupac Name 4 Chloro 4 Methylpent 2 Ene Many Mono Chloro Structural Isomers Expected Formed Free Radical Mono Chlorination Use Following Information Answer Next Question Toluene Allowed React Br2 Presence Fe Results Formati Use Following Information Answer Next Question Addition Br2 Ccl4 Ethene Results Formation Compound X Following Compounds Undergo Substitution Reaction Maximum Rate Substitution Takes Place Sn1 Mechanis School 58 Students Boys 240 Girls Find Number Boys School Rope 11 Long Two Pieces Lengths 235m 3310m Cut Length Remaining Rope Find Three Rational Numbers 4 5 Major Product Substitution Reaction One Mole Bromine Presence Febr3 Benzene Evaluate 9 8596 Evaluate 4489 Evaluate 1444 Find Square Root Number Using Method Prime Factorisation 1296 Use Following Information Answer Next Question Reaction Involving Replacement Diazonium Group Chloro Complete Given Chemical Reaction Happens N Methylaniline Heated Methyl Iodide Chloroform Stored Dark Coloured Bottles Solar System Part Galaxy Big Bang B Nebula C Saptarishi Milky Way 1 Two Ends Earth Axis Called 2 Network Parallels Meridians Called 3 Maximum Distance Two Meridians 4 Highest Court District Criminal Cases Court Judge District B Additional District C Sessions Judicial Important Determining Rightful Owner Land Policemen B District Collector C Land Records Chowkidars Maintaining Law Order District Important Responsibility District Collector B Police Officer C Pancha Fair Reserve Seats Women Sc St Gram Panchayat System Enables People Run Local Government Rural Areas Zila Parishad B Block Samiti C Pachayati Raj Solution Koh Hydrolyses Ch3chclch2ch3 Ch3ch2ch2cl One Easily Hydrolysed State Oneuseeach Ddt Iodoform Ii Compound Following Couples React Faster Sn2 Displacement 1 Bromope Write Iupac Name Given Compound Classify Following Compounds Allylic Benzylic Vinylic Halides Boiling Point N Pentyl Chloride Higher Neo Pentyl Chloride Explain Ethyl Nitrile Formed Given Reaction Give One Step Reaction Preparation Propyl Iodide Propyl Chloride Giving Reasons Arrange Following Alcohols Decreasing Order Reactivity Towards Hi Form Iodo Alkanes Name Products Formed Chlorination Methane Presence Heat B Drawback Reaction Chlorination Chlorobenzene Presence Fecl3 Give Mixture 1 4 1 2 Dichlorobenzene B Electrophilic Subst Given Compounds Compound Reactive Towards Hydrolysis Form Product Inverted Configuration Give Reason Molecular Formula Compound C6h7n Compound Treatment Sodium Nitrite Followed Cuprous Chloride Forms C Carry Following Conversions Toluene Benzyl Alcohol Ii Bromobenzene Benzene Iii Propan 2 Ol 1 Bromopr Reaction Used Preparation Flouromethane Bromomethane Beginning Toulene Write Reactions Involved Preparation P Chloro Toulene B 1 Chloro 1 Phenyl Methane P Dichloro Benzene Higher Melting Point Lower Solubility Isomers Bromobenzene Bromoethane Less Reactive Towards Nucleophilic Substitution Give Two Reasons Draw Structures Following Compounds 1 Chloro 5 Methyl Hexan 2 One Ii 2 2 Bromophenyl Ethanal B Accou Bond Enthalpy C Cl Bond Ch3cl 351 Kj Mol 1 Compared 293 Kj Mol 1 C Br Bond Ch3br Increasing Order Bond Lengths Following Compounds Give Products Formed 2 Chlorobutane Treated Alcoholic Koh B Major Product Reaction Given Compounds Ii Iii Reactivity Haloarene Increase Towards Naoh H Among Given Hydrides Hydride React Readily Ethene Hcl Hi Hbr Formation Products Reactants Requires Proper Orientation Reactant Molecules Explain Statement Citing Product Products Obtained Chlorobenzene Reacts Propyl Chloride Presence Anhydrous Alcl3 Also Write M Complete Following Reaction Iodination Benzene Carried Presence Hno3 Major Product Formed Compound Reacts Ch3ch2o Na B Given Dichloro Benzenes Highest Melting Point Different Products Obtained Ethyl Chloride Reacts Silver Nitrite Potassium Nitrite Organic Compound Molecular Formula C7h7cl Reaction Alcoholic Agno2 Gives Compound Reduction Sn Hcl G Following Compounds React Water Forming Product Inverted Configuration Draw Structure Given Compounds 1 Bromo 2 Phenyl Ethane 4 Tert Butyl 3 Iodo Heptane B Order Reactivit Write Iupac Name Given Compound Ethane Obtained Bromoethane Using Organo Metallic Compounds Draw Structures Mono Chloro Structural Isomers Expected Formed Free Radical Mono Chlorination Write One Step Method Preparation 2 4 6 Trinitrophenol 2 4 6 Trinitro Chlorobenzene B Explain Effect Organic Compound Molecular Formula C6h7n Treatment Nano2 Hcl 273 278 K Gives Intermediate B Reacts C Mechanism Involved Preparation Mixture Butan 2 Ol Butan 2 Ol 2 Bromobutane Vinyl Chloride Hydrolysed Account Following Observations Tert Butyl Chloride Reacts Aqueous Sodium Hydroxide Solution Sn1 Mech Method Preparation 1 1 Dichloro 1 Phenylethane Ethyl Benzene Complete Given Reaction B Product Obtained Aq Koh Replaced Alcoholic Koh Part Explain Chloroethane Soluble Water Benzene Give Reasons Draw Structure Products Determine Configurations Respect Reactants Given Reactions B C Choose Correct Option Regarding Chloronitrobenzene P Chloronitrobenzene B Following Names Correctly Match Reactions Iupac Name Following Compound Complete Following Reaction Gem Dihalide 1 1 Dichloroethane Hydrolysis Aq Koh Gives Compound X Upon Treatment Reagent R Forms Ye Following Compounds Maximum Boiling Point Present Asha Age Years 2 Square Daughter Nisha Age Nisha Grows Mother Present Age Asha Age Would One Reaction Alkyl Chlorides Bromides Sodium Iodide Dry Acetone Form Alkyl Iodide Known Following Halides Undergoes Sn2 Reaction Faster Use Following Information Answer Next Question Correct Order Increasing Reactivity Given Compounds S Use Following Information Answer Next Question Chlorofluorocarbon Compounds Collectively Called Freo Phosgene Common Name Use Following Information Answer Next Question Information Alternative Completes Given Equation Following Alkyl Halides Produced Swarts Reaction Correct Order Increasing Density N Propyl Halides Structure Iupac Name 4 Chloro 4 Methylpent 2 Ene Use Following Information Answer Next Question Addition Br2 Ccl4 Ethene Results Formation Compound X Many Mono Chloro Structural Isomers Expected Formed Free Radical Mono Chlorination Use Following Information Answer Next Question Toluene Allowed React Br2 Presence Fe Results Formati Bond Enthalpy C Cl Bond Ch3cl 351 Kj Mol 1 Compared 293 Kj Mol 1 C Br Bond Ch3br Write Iupac Name Given Compound Method Preparation 1 1 Dichloro 1 Phenylethane Ethyl Benzene Among Given Hydrides Hydride React Readily Ethene Hcl Hi Hbr Complete Following Reaction Among Ethane Bromoethane Compound Higher Boiling Point Methyl Iodide Turns Violet Presence Light Observed Case Methyl Chloride Following Compounds React Water Forming Product Inverted Configuration Draw Possible Enantiomer 2 3 Dimethyl Pentane Ethane Obtained Bromoethane Using Organo Metallic Compounds Chloroform Stored Dark Coloured Bottles Brown Colour Bromine Gets Discharged Br2 Added Ethene Presence Ccl4 Role Anhydrous Zncl2 Given Reaction Although Haloarenes Undergo Electrophilic Substitution Reaction Occurs Slowly Compared Benzene Write Name Reaction Used Obtaining Diphenyl Chlorobenzene Iodination Benzene Carried Presence Hno3 Given Dichloro Benzenes Highest Melting Point Classify Following Molecule Optically Active Inactive Complete Reaction Write Possible Structural Isomers Compound X C F Bond Ch3f Polar Covalent Bond Justify Statement Many Mono Chloro Structural Isomers Expected Formed Mono Chlorination 2 2 Dimethylbutane Chloroethane Soluble Water Benzene Give Reasons Iodobenzene Prepared Aniline Method Preparation 1 Bromopropane Propene Mechanism Involved Preparation Mixture Butan 2 Ol Butan 2 Ol 2 Bromobutane Vinyl Chloride Hydrolysed Slower Pace Ethyl Chloride Product Products Obtained Chlorobenzene Reacts Propyl Chloride Presence Anhydrous Alcl3 Also Write M Ch3ch2o Na Different Products Obtained Ethyl Chloride Reacts Silver Nitrite Potassium Nitrite Draw Structure Given Compounds 1 Bromo 2 Phenyl Ethane 4 Tert Butyl 3 Iodo Heptane Order Reactivities 1 2 3 Alcohols Given Reaction R Oh Hi R H2o R Alkyl Group Chloroethane Prepared Alcohols Replacement Oh Group Chlorine Atom Chlorobenzene Cannot Prepared Phen Chlorobenzotrichloride Obtained Benzyl Chloride Write One Step Method Preparation 2 4 6 Trinitrophenol 2 4 6 Trinitro Chlorobenzene Explain Effect Reactivity Chlorobenzene Nitro Group Present Meta Position Instead Para Position Tert Butyl Chloride Reacts Aqueous Sodium Hydroxide Solution Sn1 Mechanism N Butyl Chloride Reacts S Benzyl Chloride Undergoes Hydrolysis Faster Rate Chlorobenzene Complete Given Reaction Product Obtained Aq Koh Replaced Alcoholic Koh Part Explain Draw Structural Isomers C4h9br Explain Isomer Undergo Elimination Reaction Readily Chlorobenzene Reacts Koh Slower Rate Compared Chloroethane Giving Reasons Arrange Given Compounds Decreasing Order Boiling Points Butene N Butyl Iodide Ethanoic Acid Bromomethane 2 Propanol Bromopropane Aniline Bromobenzene Ethanol Flouroethane Hydrocarbon Exhibits Maximum Three Structural Isomers Straight Chain Isomer Reacting Chlorine Presen Organic Compound Molecular Formula C6h7n Treatment Nano2 Hcl 273 278 K Gives Intermediate B Reacts C Write Iupac Name Given Compound Classify Following Compounds Allylic Benzylic Vinylic Halides Boiling Point N Pentyl Chloride Higher Neo Pentyl Chloride Explain Ethyl Nitrile Formed Given Reaction Give One Step Reaction Preparation Propyl Iodide Propyl Chloride Indicate Chiral Carbon 3 Bromopent 1 Ene Reaction Used Preparation Flouromethane Bromomethane Increasing Order Bond Lengths Following Compounds Giving Reasons Arrange Following Alcohols Decreasing Order Reactivity Towards Hi Form Iodo Alkanes Name Products Formed Chlorination Methane Presence Heat Drawback Reaction P Chloro Toulene 1 Chloro 1 Phenyl Methane P Dichloro Benzene Higher Melting Point Lower Solubility Isomers Give Products Formed 2 Chlorobutane Treated Alcoholic Koh Major Product Reaction Chloroform Stored Closed Dark Coloured Bottles Give One Major Use Chloroform Chlorination Chlorobenzene Presence Fecl3 Give Mixture 1 4 1 2 Dichlorobenzene Electrophilic Substitution Reactions Haloarenes Occur Slowly Compared Reactions Benzene Given Compounds Ii Iii Reactivity Haloarene Increase Towards Naoh H Given Compounds Compound Reactive Towards Hydrolysis Form Product Inverted Configuration Give Reason Bromobenzene Bromoethane Less Reactive Towards Nucleophilic Substitution Give Two Reasons Giving Mechanism Explain Following Compounds Undergo Sn2 Mechanism Faster Rate Explain Allylic Halides Show High Reactivity Towards Sn1 Reaction Diphenyl Toluene P Chloro Acetophenone Molecular Formula Compound C6h7n Compound Treatment Sodium Nitrite Followed Cuprous Chloride Forms C Carry Following Conversions Toluene Benzyl Alcohol Ii Bromobenzene Benzene Iii Propan 2 Ol 1 Bromopr Identify X Z Following Reactions Following Structural Isomers Butyl Chloride Highest Boiling Point Product Formed Treating Propene Bromine Room Temperature Use Following Information Answer Next Question 2 Bromopropane Reacts Koh Give Compound Treated Alcoh Major Product Substitution Reaction One Mole Bromine Presence Febr3 Benzene General Form Wurtz Reaction Represented Use Following Information Answer Next Question Reaction Involving Replacement Diazonium Group Chloro Use Following Information Answer Next Two Questions According Markovnikov Rule Hydrogen Halide Added Result Markovnikov Addition Hbr 1 Phenyl Propene Major Product Following Reaction Two Chemicals X Involved Following Series Reactions X Following Compounds Produce Butan 2 Ol Reaction Ch3mgbr Result Addition Hbr 1 Phenyl Propene Use Following Information Answer Question Used Solvent Fats Alkaloids Etc Inhaling Vapours Cause Ii Use Following Information Answer Question Polyhalogen Compound Used Propellant Aerosols Also Used Me Use Following Information Answer Question Polyhalogen Compound Uses X Ccl4 Antiseptic Chi3 Ii Metal Following Structures Correctly Represents Pesticide Named Ddt Following Statements Incorrect Compound X Reagent Dipole Moment Shown Aerosol Depletes Ozone Layer Write Iupac Name Following Compound Give Reasons Following Ethyl Iodide Undergoes Sn2 Reaction Faster Ethyl Bromide Ii 2 Butanol Optical Write Iupac Name Happens Ch3 Br Treated Kcn Chlorobenzene Extremely Less Reactive Towards Nucleophilic Substitution Reaction Give Two Reasons Write Iupac Name Happens Ethyl Chloride Treated Aqueous Koh P Dichlorobenzene Higher P Isomers B Butan 2 Ol Optically Inactive Write Iupac Name Ch3 2 Ch Ch Cl Ch3 Compound Flowing Pair Undergoes Faster Sn1 Reaction Account Following C Cl Bond Length Chlorobenzene Shorter Ch3 Cl Ii Chloroform Stored Closed Dark Bro Give Iupac Name Following Compound Although Chlorine Electron Withdrawing Group Yet Ortho Para Directing Electrophilic Aromatic Substit Give Iupac Name Following Compound Although Chlorine Electron Withdrawing Group Yet Ortho Para Directing Electrophilic Aromatic Substit Give Iupac Name Following Compound Although Chlorine Electron Withdrawing Group Yet Ortho Para Directing Electrophilic Aromatic Substit Draw Structure Major Monohalo Product Following Reactions Ii Alkyl Halide Following Pair Chiral Undergoes Faster Sn2 Reaction Ii Sn1 Sn2 Reaction Occurs Inversi Write Mechanism Following Reaction Ch3ch2oh Hbr Ch3ch2br H2o B Write Equation Involved Reimer Tiema Alkyl Halide Following Pair Chiral Undergoes Faster Sn2 Reaction Ii Sn1 Sn2 Reaction Occurs Inversi Draw Structure Major Monohalo Product Following Reactions Ii Alkyl Halide Following Pair Chiral Undergoes Faster Sn2 Reaction Ii Sn1 Sn2 Reaction Occurs Inversi Draw Structure Major Monohalo Product Following Reactions Ii Write Mechanism Following Reaction Ch3ch2oh Hbr Ch3ch2br H2o B Write Equation Involved Reimer Tiema Identify Chiral Molecule Following Pair Write Mechanism Following Reaction Ch3ch2oh Hbrch3ch2br H2o Draw Structures Major Monohalo Products Following Reactions Ii B Halogen Compound Following Pairs R Identify Chiral Molecule Following Pair Write Mechanism Following Reaction Ch3ch2oh Hbrch3ch2br H2o Draw Structures Major Monohalo Products Following Reactions Ii B Halogen Compound Following Pairs R Would Undergo Sn2 Reaction Faster Following Pair Give Reasons N Butyl Bromide Higher Boiling Point Butyl Bromide B Racemic Mixture Optically Inactive Would Undergo Sn2 Reaction Faster Following Pair Give Reasons N Butyl Bromide Higher Boiling Point Butyl Bromide B Racemic Mixture Optically Inactive Would Undergo Sn2 Reaction Faster Following Pair Give Reasons N Butyl Bromide Higher Boiling Point Butyl Bromide B Racemic Mixture Optically Inactive Would Undergo Sn1 Reaction Faster Following Pair Write Structure Major Product Following Reactions Give Reasons Following Phenol Acidic Ethanol Ii Boiling Point Ethanol Higher Comparison Methoxymetha Would Undergo Sn2 Reaction Faster Following Pair Ch3 Ch2 Br Ch3 Ch2 Alkyl Halides Insoluble Water B Butan 1 Ol Optically Inactive Butan 2 Ol Optically Active C Althoug Predict Products Following Reactions Ch3 Ch Ch2 Ii 3 H2o2 Oh B2h6 Ii C6h5 Oh Br2aq Iii Ch3ch2oh Cu 5 Reactive Towards Sn1 Reaction Given Reasons C Cl Bond Length Chlorobenzene Shorter C Cl Bond Length Ch3 Cl Ii Dipole Moment Chloro Write Structure Isomer Compound C4h9br Reactive Towards Sn1 Reaction Write Structure 1 Bromo 4 Chlorobut 2 Ene Following Compounds Given 2 Bromopentane 2 Bromo 2 Methylbutane 1 Bromopentane Write Compound Reacti Write Structure 3 Bromo 2 Methylprop 1 Ene Example Benzylic Halide Following Compounds Given 2 Bromopentane 2 Bromo 2 Methylbutane 1 Bromopentane Write Compound Reacti Chlorobenzene Benzyl Chloride One Gets Easily Hydrolysed Aqueous Naoh Define Ambident Nucleophile Example Ch3 3c Br Ch3 3 C One Reactive Towards Sn1 Ii Write Product Formed P Nitrochlorobenzene Heated Aque Write One Stereochemical Difference Sn1 Sn2 Reactions Write Structures Main Compounds B Following Reactions Arrange Following Increasing Order Base Strength Gas Phase C2h5 3n C2h5nh2 C2h5 2nh Monochloro Derivative Pentane Chiral Write Name 1 1 1 Trichloro 2 2 Bis 4 Chlorophexyl Ethane Popularly Known One Following Reagents Acceptable Preparing Chloroalkanes Alcohols Socl2 Hcl Pcl5 Pcl 3 Assertion Benzyl Bromide Kept Acetone Water Produces Benzyl Alcohol Reason Reaction Follows N2 Mecha Assertion Boiling Point Alkyl Halide Decrease Order Ri Rbr Rcl Rf Reason Fluorine Electronegative At Give Method Preparation Ethanoic Acid Propanoic Acid B Predict Product Formed Hoffmann Bromamide Deg Giving Reasons Arrange Given Compounds Decreasing Order Boiling Points Undergo Sn1 Reaction Faster Oh Conversion Alkyl Halide Alcohol Aqueous Naoh Classified Dehydrohalogenation Reaction B Substitution Conversion Methyl Chloride Methyl Fluoride Known Finkeltein Reaction B Swarts Reaction C Williamson Write Chemical Reactions Chlorobenzene Respect Sulphonation B Acetylation C Nitration Action Following Ethyl Bromide Alcoholic Solutions Potassium Hydroxide Ii Moist Silver Oxide Iii Sil Read Passage Given Answer Following Questions Sn1 Reaction Substitution Nucleophilic Unimolecular Re Identify Following Reaction 2na Dryether 2 2 5 5 Tetramethylhexane 2nabr 2 Bromo 2 Methylbutane B L Compound Ethane B Propane C N Butane N Pentane Define Racemic Mixture Give Iupac Name Explain Mechanism Alkaline Hydrolysis Tert Butyl Bromide Energy Profile Diagram Define Carbolic Acid Chlorobenzene Prepared Aniline Chlorobenzene Converted Diphenyl Select Write Appropriate Answers Given Alternatives Preparation Alkyl Fluoride Alkyl Chloride Presen Correct Iupac Name Given Compound Following Reagents Used Preparation Alkyl Fluorides Alkyl Chlorides Bromides Following Question Statement Assertion Followed Statement Reason Choose Correct Answer Following Cho Reaction Leads Production Grignard Reagent Products Obtained Reaction Chlorobenzene Conc Hno3 Conc H2so4 Chemical Formula Poisonous Gas Obtained Oxidation Chloroform Following Alkyl Bromides Reactive Towards Sn2 Reaction Substitution Primary Alkyl Chloride Nucleophile Takes Place Step Substitution Tertiary Alkyl Chlorid Correct Order Reactivity Alkyl Halides Towards Nucleophilic Substitution Reactions Product Obtained Sn2 Reaction Asymmetric Compound Always