Nucleophilic Substitution Reaction - NUCLIEOPHILIC SUBSTITUTION REACTION 1 The nucleophile has a 2 What is the molarity of the HCl used in this

Nucleophilic Substitution Reaction - NUCLIEOPHILIC...

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NUCLIEOPHILIC SUBSTITUTION REACTION 1.The nucleophile has: 2.What is the molarity of the HCl used in this experiment? 3.How many mL of 2-methyl-2-butanol should you use? 4.Why do you have to open the stopcock of the sep funnel eachtime after shaking the reaction mixture? 5.If one gets acid in the eye: 6.The product of today's experiment is: 7.The product of the reaction in the sep funnel is: 8.After successful completion of the reaction one must rinse the organic layer with:
9.After successful completion of the reaction one must rinse the organic layer with: 10.The synthesized and rinsed product must be dried over: 11.To obtain the boiling point of your unknown you must perform: 12.How many test tubes do you need in part 2 of this experiment? 13.1-chlorobutane is also known as: 14.2-chlorobutane is also known as: a.sec-Butyl chloride 15.t-Butyl chloride is also known as a.2-chloro-2-methylpropane 16.n-Butyl bromide is also known as:
a.1-bromobutane 17.3-chloropropene is also known as: a.Allyl chloride 18.Chlorobenzene is also known as: a.chlorinated benzene 19.On what position, to what carbon, is the -OH group attached in the t-amyl alcohol? a.Second 20.If no precipitation is observed in a reaction tube you should heat it to: a.50-55 C 21.In what outlet should you plug in your sand bath? a.10 A 22.To what setting should you adjust the rheostat for your sand bath? a.60 23.In part B of your second experiment you should put 2 mL of what 15% solution in your test tubes? a.NaI
24.In Sn1 reaction the HCl serves two roles: a.It is both the nucleophile and the catalyst 25.In Sn1 reactions the -OH has the best properties of leaving group when it is: a.Connected to a primary carbon

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