Draw the line angle formulas for all products obtained when the following compound is subjected to ozonolysis using excess ozone with reductive work-up.
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- Complete the mechanism for the formation of the major species at equilibrium for the reaction of butanal in methanol solvent and catalytic aqueous acid. Make sure to include any missing atoms, bonds, charges, nonbonding electrons, and curved arrows.Which of the following is statements is/are TRUE about the experiment on the relative rates of electrophilic aromatic substitution?I. The experiment must be performed in dark conditions. II. Using the same solvents, a faster decolorization will be observed in aniline as compared to ethylbenzene. III. Chlorobenzene will react faster than methoxybenzene. IV. The use of AlCl3 in the halogenation of aromatic compounds using elemental bromine could hasten the reaction.Write a essay summarizing details and analysis of proofs for identification test for Qualitative Tests for carbonyls and Unknown carbonyl resulting in the finalUnknown, which is benzaldehyde.
- Write the overall balanced equation for the transformation of bromobenzene into benzoic acid through a Grignard reaction. Include all reagents and products but not solvents. Draw a detailed mechanism for the same process, making sure to indicate clearly the starting and ending points of all arrows and charges where needed.Make an experimental step-by-step procedure with regards to the synthesis of Butyl Acetate shown below. Please make it detailed and tell the equipment used in the process. Thank you!(Give clear handwritten solution) give reaction mechanism and major product for the all three subparts (a,b and c) solution.
- i. Provide a detailed, stepwise, and balanced mechanism that accounts for the observed product and byproducts. ii. The chemistry that occurred happened selectively. What are two other unique and reasonable ways that molecule could have reacted but didn’t?Why is methanol chosen as the solvent for recrystallization? What would happen if the student uses dichloromethane instead? The reaction is Electrophilic Aromatic Substitution: Friedel-Crafts Alkylation. More info attachedWhat are several products for the following reaction with mechanisms included?
- Give the reaction mechanism for both subparts in clear handwritten paper!can you please provide the curved arrow mechanism for the first halogenation reaction of a positive iodoform test with acetone. also please provide the final products of the positive iodoform test with acetone.Given the sequence of reactions shown below assume the reactions are stoichiometric fill in the reagents needed for steps A B and C and explain what happens in each step of the reactions, by also name