Interpretation:
Conversion of toluene to 3-hydroxybenzoic acid has to be shown.
Concept introduction:
Nitration: In nitration reaction, one nitro group
Oxidation: If electrons are moved from a species or oxygen atoms are added to a species or hydrogen atom gets removed from a species during a
Conversion of
Aromatic amines converted to arenediazonium salt by reacting with
Reduction: If electrons are gained to a species or hydrogen atoms are added to a species or oxygen atom gets removed from a species during a chemical reaction is known as reduction. In a reaction,
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Chapter 23 Solutions
Organic Chemistry
- Show how to convert ethylene to Ethane compound.arrow_forwardShow the complete synthesis for the following reaction that forms the following product(s) PLEASE INCLUDE STRUCTURE AND REAGENTarrow_forward3. Complete the following reactions - draw the reactants and products, show the mechanism and conditions, and name the products. These reactions are one step. a) 2-Propanol + butanol → b) Ethanol + [O] → c) Butanone + [H] → d) 2-pentene + H₂O → e) Ethene + H₂ →→ f) Pentanol + HCI → g) Methanoic acid + 2-butanol → h) aminoethane + hexanoic acid → i) Benzene + chloroethane →→ j) Octane + O₂ → 2arrow_forward
- Starting with ethene give a suitable reaction scheme to convert it into Ethyl ethanoate in 4 stepsarrow_forwardAlkynes do not react directly with aqueous acid as do alkenes, but will do so in the presence of mercury(II) sulfate as a Lewis acid catalyst. The reaction occurs with Markovnikov regiochemistry, so the OH group adds to the more highly substituted carbon and the H adds to the less highly substituted carbon. The initial product of the reaction is a vinyl alcohol, also called an enol. The enol immediately rearranges to a more stable ketone via tautomerization. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions -X티 Hö: H-O -CH3 -CH3 H30*arrow_forwardThe addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically favored. What would be the product for the reaction above? Hint: Think of the self-ionization of water and the polarity of the carbonyl group.arrow_forward
- Draw out the mechanism pleasearrow_forwardTo prepare the ethyl butanoate compound, which has pineapple aroma, ethanol is used as one of the starting reagents. Which other reagent is suitable to obtain this product, show the mechanism.arrow_forwardWhen ethoxybenzene is treated with a mixture of nitric acid and sulfuric acid, two products are obtained, each of which has the molecular formula C8H9NO3. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph.arrow_forward
- draw out the reaction as well as the mechanism for the reaction of methyl iodide and para-ethylphenol. Be sure to label the final productarrow_forward1. b) Show the MECHANISM for the POLAR addition of molecular chlorine to cyclopentane. c) The reaction of toluene and ethylbenzene was through the alkyl groups, -CH 3 and -CH 2 CH 3, respectively. Why didn’t xylene, which has TWO methyl groups, react with bromine in the time allotted?arrow_forwardQ.11arrow_forward
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