Draw the Major Organic product of the following reaction. Do NOT use abbreviations such as Ph. Do NOT draw out any hydrogen explicitly. Do NOT include the ionic side product or any other side product such as water, CH3NH2 or CH3NH3+. (i) p-Toluidine + Br₂ (excess) H₂O Draw Your Solution
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- Draw the major product of this reaction. Ignore inorganic byproducts. 1.NaBH4 2. Neutralizing work-upIn the following reaction Series, write down the appropriate reagents that can be used where there are question marksSeveral reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
- Complete the reactions below using the required reagents or products. If there is no reaction, indicate so. If a product is in the majority, specify which one.In the reaction series below, write down the appropriate reagents that can be used where there are question marks.Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acid
- show the missing reagents and intermediates in the reaction sequence belowChemistry Show retro-synthetic analysis leading from the target molecule to the precursor molecule showing all intermediate molecules.Using organic chemistry from your textbook show an efficient synthesis of your target molecule starting from its parent molecule and showing the structure of each isolable intermediate.Assume you have access to usual reagents like Br2, AlCl3, Fe, HBr, HNO3, H2SO4, etc.Assume that each intermediate can be purified from other products at each step of the synthesis.Fill in the appropriate reagents to best accomplish the reaction shown OR fill in the missing products. Identify the major and minor products if applicable.
- For SN1 Explain the order in which 2o (secondary) alkyl halides reacted (fastest to slowest) and explain why. 2o (secondary) compounds listed are: (see picture) 2-chlorobutane 2-bromobutane bromobenzene bromocyclopentane bromocyclohexane Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature. Be sure to explain which alkyl halides did not react and whyDraw mechanisms for the following reactions. Use curved arrows to showelectron flow for each step and draw out all reactants to effectively show all arrow pushing. Be sure to pay attention to pKa values and avoid mixed media!Minor product via E1 for 2-butanol and HCl?