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- Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. The aromatic ring, when present, is unreactive in all cases. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.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?Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
- Draw the major organic product(s) of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.Draw a structural formula for the major organic product of the reaction shown. You do not have to consider stereochemistry. If there is more than one major product possible, draw all of them. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.How combination of Br2 and H2O effectively forms bromohydrinsfrom alkenes ?
- Add reactants, reagents and products. Include the stereochemistry if necessary. Unless otherwise stated, assume the reagents are in excess.Ethers: Reaction of 1-methoxy-2- methylpropane and HI, heat. Draw the organic product or products formed when the structure shown below is heated with HI. If no reaction occurs, draw the starting material. Interactive 3D display modeDraw the major product of this reaction. Ignore inorganic byproducts. PCC, CH2Cl2
- Fill in the missing reactant, reagent and products. Indicate stereochemistry if necessary. Unless otherwise specified, assume the reagents are in excess.1.Build a carbon chain of 9 carbon atoms, which has an alkene, an alcohol, an amine. Please name according to the IUPAC nomenclature. 2.Build an 8-point cycle, which has a ketone and a carboxylic acid. Please name according to the IUPAC nomenclature.A 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.