/10 Report a question What's wrong with this question? You cannot submit an empty report. Please add some details. 12345678910 Chapter 6 : Haloalkanes and Haloarenes This Quiz Contains a set of 10 Questions. The Passing Cut-off is 60%. To start the Quiz, click on the Start Button. All the Best! 1 / 10 Which compound undergoes substitution fastest in aqueous medium? CH₃Cl C₂H₅Cl sec-butyl chloride tert-butyl chloride 2 / 10 Which compound undergoes elimination most easily? Primary Secondary Tertiary Aryl 3 / 10 Vicinal dihalides have halogens on same carbon adjacent carbons terminal carbon aromatic ring 4 / 10 The reaction of haloalkane with KCN gives nitrile alcohol amine alkene 5 / 10 In SN1 reaction, rate depends upon substrate nucleophile solvent temperature only 6 / 10 Which of the following undergoes SN1 reaction fastest? CH₃Cl CH₃CH₂Cl (CH₃)₂CHCl (CH₃)₃CCl 7 / 10 Order of boiling point of halomethanes is CH₃Cl > CH₃Br > CH₃I CH₃I > CH₃Br > CH₃Cl CH₃Br > CH₃Cl > CH₃I CH₃Cl > CH₃I > CH₃Br 8 / 10 Correct order of C–X bond strength is C–I > C–Br > C–Cl > C–F C–F > C–Cl > C–Br > C–I C–Br > C–Cl > C–I > C–F C–Cl > C–F > C–Br > C–I 9 / 10 SN1 reaction proceeds via carbocation carbanion free radical concerted step 10 / 10 Which compound is least reactive towards nucleophilic substitution? CH₃Cl C₂H₅Cl vinyl chloride tert-butyl chloride Your score is 0% Restart quiz
