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A: Answer shown in attachment provide in explanation box Explanation:
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- True or False: 1. If the reactants are more stable than the products, the reaction will be spontaneous. 2. The first substituent should have the higher number in numbering the longest chain.When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?Identify an electrophile from the following list A. CH3- B. NH3 C. BH3 D. None of these
- Draw the major organic product formed when the compound shown below undergoes a reaction with (CH3CH2)2NH under acidic conditions.draw the organic products you would expect to isolate, from the following reactions (after hydrolysis)In the presence of heat or light, diazomethane is converted into a carbene that adds to alkenes. Draw the correct products for the following reaction. Please draw stereochemistry at all chiral centers ( 2 flat bonds, 1 dash and 1 wedge).
- Write the products of the compound and the following reagents. If the reaction would not work for your compound, write "no reaction" and explain the problem. CrO_3The product of the second synthetic step undergoes tautomerization in aqueous medium to form the final product. Draw the structures for both of these products. 1. Draw the product of the oxidation of the organoborane formed in Step 1. Include lone pairs and nonzero formal charges. 2. Draw the more stable tautomer that is the final product. Include lone pairs and nonzero formal charges.Consider a reaction where cis-but-2-ene is treated with a peroxy acid followed by OH- /H20. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- For the following step in a reaction, use arrows to show how the end product is achieved.Organic Chemistry 1. EA27. Please explain why B. letter is the answer, and not A, C, or D letters ? ThanksA hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.