1.Why does benzyl bromide react under both SN1 and SN2 conditions? Why is bromobenzene unreactive under...

1.Why does benzyl bromide react under both SN1 and SN2 conditions? Why is bromobenzene unreactive under both SN1 and SN2 conditions?

2. If bromobenzene reacts faster than chlorocyclohexane in an SN2 reaction, what could be the reason?

Expert Solution

queen_honey_blossom answered 2 years ago

Draw the Sn1 intermediate and Sn2 transitions state for both ethyl-2-chloroacetate and benzyl bromide (α-bromotoluene). Use...

Draw the Sn1 intermediate and Sn2 transitions state for both ethyl-2-chloroacetate and benzyl bromide (α-bromotoluene). Use these structures to explain the differences in reactivity between these two compounds.

Which of the following produces the most stable carbocation? allyl bromide 2-bromo-2-methylpropane bromobenzene benzyl bromide

Write equations for the reactions investigated. Label Sn1 or Sn2. 1)Butyl bromide in 15%NaI-acetone 2)Butyl bromide...

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In what ways does an organization react to change? Under what conditions are the members of...

In what ways does an organization react to change? Under what conditions are the members of an organization likely to embrace and accept change? Under what conditions are they likely to resist change?

Question about SN1 and SN2 reactions. In my lab we prepared 1-bromobutane from 1-butanol (SN2) and...

Question about SN1 and SN2 reactions. In my lab we prepared 1-bromobutane from 1-butanol (SN2) and 2-chloro-2-methylbutane from 2-methyl-2-butanol (SN1). I don't undetstand the following questions: 1. Why did we heat the SN2 reaction but not the SN1 reaction? 2. What was the purpose of performing a simple distillation on both reactions? What were you isolating your products from? 3. What was the purpose of washing both of oyur reaction mixtures with brine (saturated sodium chloride)?

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What role does the leaving group play on the rate of SN1 versus SN2 reactions? (compare 1-bromo to 1 chloro, 2-bromo to 2-chloro etc).What role does the structure of the substrates play on the rate of SN1 versus SN2 reactions (compare primary,secondary and tertiary that may have the same leaving group) where is the chiral carbon located?

1. Define and describe what is meant by Sn1 and Sn2. 2. Describe the differences between...

1. Define and describe what is meant by Sn1 and Sn2. 2. Describe the differences between Sn1 and SN2 reactions, including mechanistic details. 3. Discuss the difference between the intermediates for each mechanisms- which you should draw.

1) Create a chart comparing E1, E2, SN1 and SN2 reactions. Be detailed and cover: structure...

1) Create a chart comparing E1, E2, SN1 and SN2 reactions. Be detailed and cover: structure of RX, reactivity of nucleophile, concentration of nucleophile, solvent and stereochemistry.

ORGANIC CHEMISTRY experiment : Synthesis of n-butyl bromide (Sn2) 1.what is the function of the Hickman...

ORGANIC CHEMISTRY experiment : Synthesis of n-butyl bromide (Sn2) 1.what is the function of the Hickman Still in this experiment? 2. what is the function of the condenser in this experiment?

SN2 Reactions of Alkyl Halides 1.a) Which alkyl bromide reacted fastest with sodium iodide in acetone:...

SN2 Reactions of Alkyl Halides 1.a) Which alkyl bromide reacted fastest with sodium iodide in acetone: 1-bromobutane, 2-bromobutane or 2-bromo-2-methylpropane? b) Which alkyl bromide reacted slowest? Explain how the structure of the alkyl halide affects the rate of an SN2 reaction. 2. a)Which alkyl bromide reacted faster with sodium iodide in acetone: 1-bromobutane or 1-bromo2,2-dimethylpropane (neopentyl bromide)? b)Both of these are primary halides. Why was there a difference in reactivity? 3.a)Which halide reacted faster with sodium iodide in acetone: 1-bromobutane...

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