When the (R,R) isomer of the amine shown is treated with an excess of methyl iodide, then silver oxide, then heated, the majorproduct is the Hofmann product.) Some Zaitsev product is also formed. It has the (E) configuration. When the same amine is treated with mCPBA and heated, theZaitsev product has the (Z) configuration. Use stereochemical drawings of the transition states to explain these observations

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When the (R,R) isomer of the amine shown is treated with an excess of methyl iodide, then silver oxide, then heated, the major
product is the Hofmann product.
) Some Zaitsev product is also formed. It has the (E) configuration. When the same amine is treated with mCPBA and heated, the
Zaitsev product has the (Z) configuration. Use stereochemical drawings of the transition states to explain these observations

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