2. Complete the road map by providing the structures of the products or the reagents as needed in the boxes provided below. Please note, there may be more than one reagent needed for some of the steps. H HSCH2CH2CH2SH AICI3 or BuLi 1. 2. H3O+ H3O+ H2CrO3 HgO, H₂O, H+
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- Complete the road map by providing the structures of the products as needed in the boxesprovided below. Please note, there may be more than one reagent needed for some of thesteps.Complete the road map by providing the structures of the products or the reagents as neededin the boxes provided below.Complete the reactions below by providing the proper structure(s) in the boxes. Include stereochemistry wherever necessary. The structures only, no need to draw mechanisms
- Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.Propose a detailed mechanism for the reaction below (in the attached picture), showing the structure of thestable intermediate and using curved arrows to indicate electron flow in each stepSynthesis of 3-Methylbutyl Ethanoate by an Acid Catalysed Esterification (FischerEsterification) & Purification by Simple Distillation Can you explain the details of what's going on this reaction please Specifics please i'll also leave a good review if you can help thank you
- For each of the following reactions,provide the major product(s) or the necessary reagents to perform the chemical transformations indicated. If no reaction takes place, write NR.the reactions should be all covered in organic chemistry loudon 6 th edition , for exmaple, clemensen/wolf -kishner. acylate etc.Provide a detailed mechanism for the following (Hint:halohydrin reaction). Use arrows to show electron flow and show intermediates.An elimination step is involved in the synthesis of aromatic amino acids. We can also envision this occurring in a laboratory setting with a strong base. Provide a 1 step mechanism for this decarboxylation reaction. Note: under strongly basic conditions, hydroxide is a reasonable leavinggroup.