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List the three requirements for a substitution reaction to proceed via the SN1 mechanism.
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- Write an introduction on the ferrocene molecule, describing it's structure. What would happen if ferrocene was acetylated. Discuss the two products that may be formed due to the attachment of the acetyl group. Draw this in a reaction mechanism.Describe the principle and mechanism behind the catalytic hydrogenation of alkenes using a heterogeneous catalyst. Explain the factors that influence the reaction rate and selectivity in this process.C5H8 + 7O2 → 5CO2 + 4H2O type of reaction
- The SN2 type reaction will end up with the substitution 2903 the at the reaction center of the reaction. 903 182903 SEY 9037In the second paragraph you should explain why 2-chloro-2-methylpropane reacts with water via the SN1 mechanism instead of the SN2 mechanism, and then write the steps in the mechanism for this reaction. Then write the balanced equation for the reaction between 2-methyl-2-chloropropane and water. One of the products of this reaction is HCl. The rate at which HCl is produced is equal to the rate at which 2-chloro-2-methylpropane is consumed. In this experiment, the HCI will be neutralized by incremental addition of a sodium hydroxide solution. Write the balanced equation for the reaction between NaOH and HCI.Define the Mechanism of the Radical Addition of HBr to an Alkene ?
- Predict the product of the following organic reaction: CH₂ CH O || C–CH2–CH=CH—(CH2)3 CH3 (CH₂)3 CH=CH- - CH₂ CH3 + 4 H₂ Ni CH,−O -C–CH2–CH=CH–CH=CH–CH2–CH3 Specifically, in the drawing area below, draw the chemical structure of the product P. If there is no product, because this reaction won't happen, check the No reaction box under the drawing area. Click and drag to start drawing a structure. × Ś +Write a mechanism for this reaction: Br Br₂ H2O + ОН Br OH13) OEt i) LDA 2) CHO