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- What reaction category/mechanism type does the following reaction fit? O addition substitution (SN1) substitution (SN2) O elimination (E1) O elimination (E2) HCI CI + HOPleas explain how this process occurs. Identify SN1, SN2, E2, E1, nucleophiles and electrophiles.When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.
- What is(are) the product(s) of the following hydroboration-oxidation reaction? Include stereochemistry.Write the products of the following aromatic electrophilic substitutionsUnder what reaction conditions does the electrophilic chlorination of aromatic compounds usually occur? Cl₂, H₂O NaCl, H₂O Cl2, CC14 Cl2, FeCl3 NaCl, CH3OH
- Classify the following species as electrophiles or nucleophiles Please explainDraw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. D xx + H₂O + X Click and drag to start drawing a structure.For the reaction below identify the reactant electrophile and the nucleophile.
- Draw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. SH + 0 Br + X S C Click and drag to start drawing a structure.Which of the following is the most feasible reactant for the synthesis of 1-Bromo-1-methyl cyclohexaneThe mechanism for the synthesis of biodiesel is not a nucleophilic aryl substitu OGMU 2020 749692 O True O False

