CH3OH is the nucleophile found in the reaction mechanism on the pre-lab lecture slides.
A chemical species known as a nucleophile in chemistry creates bonds by giving up a pair of electrons. The term "nucleophile" refers to any molecule or ion containing a free pair of electrons or at least one pi bond. Nucleophiles are Lewis bases because they donate electrons.
The term "nucleophilic" refers to a nucleophile's propensity to form bonds with positively charged atomic nuclei. Nucleophilicity, also known as nucleophile strength, describes a substance's nucleophilic properties and is frequently used to compare the atoms' affinities. Solvolysis refers to neutral nucleophilic reactions with solvents like water and alcohols. Nucleophiles can engage in nucleophilic addition and substitution, whereby a nucleophile is drawn to a full or partial positive charge. Basicity and nucleophilicity are strongly connected.
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