(a)
To determine: The effect on the reaction rate if the concentration of ethanol gets doubled in the given reaction of tert-butyl ether and ethanol.
Interpretation: The effect on the reaction rate if the concentration of ethanol gets doubled in the given reaction of tert-butyl ether and ethanol is to be predicted.
Concept introduction: The replacement or substitution of one functional group with another different functional group in any
The nucleophilic reaction contains only a substrate as a reactant not a nucleophile which means a unimolecular nucleophilic reaction is termed as
(b)
To determine: The effect on the reaction rate if the concentration of tert-butyl ether gets tripled and the concentration of ethanol gets doubled in the given reaction.
Interpretation: The effect on the reaction rate if the concentration of tert-butyl ether gets tripled and the concentration of ethanol gets doubled in the given reaction is to be predicted.
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. There are two types of substitution reaction. First one is electrophilic substitution reaction in which electrophile is present as a reagent and second one is nucleophilic substitution reaction in which nucleophile is present as a reagent.
The nucleophilic reaction contains only a substrate as a reactant not a nucleophile which means a unimolecular nucleophilic reaction is termed as
(c)
To determine: The effect on the reaction rate if the temperature of the given reaction gets raised.
Interpretation: The effect on the reaction rate if the temperature of the given reaction gets raised is to be predicted.
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. There are two types of substitution reaction. First one is electrophilic substitution reaction in which electrophile is present as a reagent and second one is nucleophilic substitution reaction in which nucleophile is present as a reagent.
The nucleophilic reaction contains only a substrate as a reactant not a nucleophile which means a unimolecular nucleophilic reaction is termed as
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Organic Chemistry (9th Edition)
- When tert-butyl bromide is heated with an equal amount of ethanol in an inert solvent, one of the products is ethyl tert-butyl ether. (a) What happens to the reaction rate if the concentration of ethanol is doubled?arrow_forwardwhich will proceed more easily at room temperature the bromination of cyclohexene or the bromination of benzene?arrow_forwardWhen ethyl bromide is added to potassium tert-butoxide, the product is ethyl tert-butyl ether. What happens to the rate if the temperature is raised?arrow_forward
- Fill in the missing reagents in the boxes below. some steps may require more than one step.arrow_forwardIn an SN2 reaction between 2-chlorobutane and iodide ion, what happens to the rate of the reaction if: (a) the concentration of 2-chlorobutane is doubled? (b) the concentration of iodide is doubled?arrow_forwardIn each reaction box, place the best reagent and conditions from the list below.arrow_forward
- The reaction product below is a vinyl halide. Considering the vinyl halide formation reaction, what happens to the reaction rate if the hydrogen halide concentration is doubled and the hydrocarbon concentration remains constant? doubles the speed of vinyl halide formation quadruples the rate of formation of vinyl halide triples the speed of formation of vinyl halide doubles the rate of hydrogen halide formation naharrow_forwardA student wanted to know whether the greater proximity of the ucleophile to the C-2 carbon in the transition state is what causes the 1,2-addition product to be formed faster when 1,3-butadiene reacts with HCl. Therefore, she decided to investigate the reaction of 2-methyl-1,3-cyclohexadiene with HCl.Her friend told her that she should use 1-methyl-1,3-cyclohexadiene instead. Should she follow her friend’s advice?arrow_forwardConsider the reaction of NaCN with 1-bromohexane in DMSO. Predict the change in rate of reaction if the concentration of the NaCN is tripled. A) The reaction rate stays the same B) The reaction rate doubles C) The reaction rate is halved D) The reaction rate quadruples E) The reaction rate triplesarrow_forward
- The reaction of an amine with an alkyl halide gives an ammonium salt. The rate of this SN2 reaction is sensitive to the polarity of the solvent. Draw an energy diagram for this reaction in a nonpolar solvent and another in a polar solvent. Consider the nature of the transition state, and explain why this reaction should be sensitive to the polarity of the solvent. Predict whether it will be faster or slower in a more polar solvent.arrow_forwardWhat happens in the rate-limiting step of the reaction? a) The bromide ion detaches from the alkyl halide and a carbocation intermediate is formed b) Ethanol attacks the alkyl halide carbon and replaces the leaving group c) The speed-limiting step is unknown d) Ethanol is associated with a carbocationarrow_forwardWhen ethyl bromide is added to potassium tert-butoxide, the product is ethyl tert-butyl ether. (a) What happens to the rate if the concentration of potassium tert-butoxide is tripled and the concentration of ethyl bromide is doubled?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning