Determine the mechanism and product for the given reaction by adding atoms, bonds, nonbonding electron pairs, and curved arrows. Acid and water are added in the second step. H CH₂CH₂MgBr product

You determine the bimolecular rate constant k for a set of SN2 reactions. Based on your understanding of how the nucleophile effects the rate constant for an SN2 reaction, drag and drop the nucleophiles into the correct rows in the table below. Alkyl halide Nucleophile k / L mol-1 s-1 CI 0.011 -CI 0.045 0.074 0.095 -NH2 -NH2 >-NH2 -NH2 -NH2

8. Compound (A) rearranges to compound (B) spontaneously. a) Draw the mechanism using curved arrows, that describes how this rearrangement can occur. (Hint: two shifts are required to obtain the product). H Br H₂C Br b) What makes the formation of the previous product spontaneous (ie. why is the product more stable than the reactant)?

HO .OH cat. H2SO4 H₂O cat. H2SO4 Complete both mechanisms above. BRIEFLY explain how the different reaction conditions (in the presence of acid) result in different products being formed. How does equilibrium play a role?

Draw all of the steps of the mechanism for this reaction. You do not need to show curved arrows for the step involving Mg metal. os Br OCH₂ Mg Et₂0 "MgBr "OCH3

Draw a detailed arrow pushing mechanism for the following reaction. In the rate-determining step unimolecular (SN1) or bimolecular (SN2)

In an SN2 mechanism, how does it work, what are all of the steps, transition state and all final products?

Please answer this organic chemistry question: show all three steps and radical mechanism for hydrobromic acid in peroxide reacting with 3-methylene-2-ene. Are there multiple products?   Background information just in case needed for the intial question above ? but if not needed  just ignore this background information: which of the following compounds will react the quickest? A) Fluorine with a tertiary radical  B) chlorine with a tertiary radical  C) Bromine with tertiary radical  D) chlorine with a primary radical  E) bromine with a primary radical

Draw the mechanism arrows for both propagation steps for the radical addition of HBr to the alkene.

Write mechanisms for each reactions.