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1.arrange the following alkyl halides in the order of the rate of their reaction

ID: 986470 • Letter: 1

Question

1.arrange the following alkyl halides in the order of the rate of their reactions with iodide( from fastest to slowest) a. 1-chlorobutane b)1-bromobutane c. 2-chlorobutane d. 2-bromobutane e. 2-bromo-2-methylpropane f. Bromobenzene
2. Predict the stability of the carbocation resulting from the reaction AgNO3 in ethanol with the following Alkyl halides (least to most stable carbocation) a. 2-bromobutane b. 2-bromo-2-methylpropane c. 2-bromobutane d. Allyl bromide

3. Write mechanism for conversion of triphenylmethyl to trityl methyl ether using conc H2SO4 and methanol . Draw box around key intermediate and name mechanism 1.arrange the following alkyl halides in the order of the rate of their reactions with iodide( from fastest to slowest) a. 1-chlorobutane b)1-bromobutane c. 2-chlorobutane d. 2-bromobutane e. 2-bromo-2-methylpropane f. Bromobenzene
2. Predict the stability of the carbocation resulting from the reaction AgNO3 in ethanol with the following Alkyl halides (least to most stable carbocation) a. 2-bromobutane b. 2-bromo-2-methylpropane c. 2-bromobutane d. Allyl bromide

3. Write mechanism for conversion of triphenylmethyl to trityl methyl ether using conc H2SO4 and methanol . Draw box around key intermediate and name mechanism
2. Predict the stability of the carbocation resulting from the reaction AgNO3 in ethanol with the following Alkyl halides (least to most stable carbocation) a. 2-bromobutane b. 2-bromo-2-methylpropane c. 2-bromobutane d. Allyl bromide


3. Write mechanism for conversion of triphenylmethyl to trityl methyl ether using conc H2SO4 and methanol . Draw box around key intermediate and name mechanism

Explanation / Answer

1. 2-bromobutane > 2-chloro butane > 1-bromo butane > 1-chloro butane > 2-bromo 2-methyl propane > bromo benzene

2. allyl bromide > 2-bromo 2-methyl propane > 2-bromo butane

3. both starting material and product are same pls check