Concept explainers
Synthesize each compound from the given starting material. You may use any other required inorganic reagents.
a. c.
b. d.
e.
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Organic Chemistry - With Access (Custom)
- taken in order to gor the product Please explain the mechanisms/stepsarrow_forwardB. Draw structures for the products in the following reactions. my NH₂ NH₂ 1. LIAIH4 2. H₂O* xs EtBr 1. Mel 2. Ag₂O, H,O, heat acetone, formaldehyde cat. HCIarrow_forward9. What is the major organic product obtained from the following reaction? 1. BH3 2. H₂O₂, NaOHarrow_forward
- Which reagent(s) convert a carbonyl group (C=O) into a methylene group (CH2)? O A. Zn / HCI O B. LIAIH4 / Et20 O C. NABH4 / MeOH D. Na in liq. NH3arrow_forwardDraw the structure of a dihalide that could be used to prepare each alkyne. There may be more than one possible dihalide. CH3 b. CH₂-C-C=CH CH₂ a. CH₂C=CCH₂ C. -C=C-arrow_forward18. Ketone reduction Dicyclohexyl ketone Reduce the ketone. 1. NaBH4, ethanol 2. H3O+ H OH Dicyclohexylmethanol (88%) (a 2° alcohol)arrow_forward
- Does the equilibrium favor the reactants or products in each substitution reaction? a. CH;CH2-NH2 Br CH;CH2-Br + "NH2 b. "CN CN + I-arrow_forwardComplete each hydrogenation reaction. catalyst a. CH2=CH-CH3 + H2 catalyst b. CH3-CH-CH=CH2 + H2 ČH3 catalyst c. с. CH, —CH—С—СH, + H, ČH; ČH;arrow_forwardH. An ester is produced by the reaction of an alcohol with a carboxylic acid. For each ester below, underline the alcohol part and circle the carboxylic acid part. Then, name each ester. CHỊCH,CH,CH,CH,-O-C-CH,CH,CH, H CH₂ CH₂ CH 1 CH3arrow_forward
- Complete the following halogenation reactions for alcohols. Draw the structure of the product. Name the reactant and the product. a) Cty-CH-0H b) CH3 CH-CH-CH PBY3 c) PE 7. Name the following phenols. d) a) b) OH c) OH Br OH CH2 HO CI Br 8. Name the following ethers. b) a) CHy-0-C-CHs CHy-0-CH3 c) d) Cy-CH-0 talamc) Earrow_forward16. Identify each compound as an a cohol, a phenol, or an ether. Classify any alcohols as primary (1"), secondary (2), or tertiary (3"). a. CH,CH,CH,OH CH,CHCH, b. CHO C. CH CHOCH, CH, d.arrow_forward3. Ethanoic acid (vinegar) when diluted to low concentrations by water can be prepared from ethene by a) reduction with H2, followed by reaction with a strong oxidizer b) addition of HCL followed by reaction with H20 c) addition of H20 followed by reaction with a strong oxidizer d) addition of Br2 e) followed by reduction with H2arrow_forward
- Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning