When ethyl bromide reacts with potassium cyanide in methanol, the major produce is
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- Reaction of iodoethane with CN- yields a small amount of isonitrile, CH3CH2N≡C, along with the nitrile CH3CH2N≡N, as the major product. Write electron-dot structures for both products, assign formal charges as necessary, and propose mechanisms to account for their formation.arrow_forward(b) (1-chloromethyl)cyclopentane, C6H11CI reacts with aqueous sodium hydroxide, NaOH to produce a primary alcohol AA. When CsH11Cl is added with magnesium, Mg in ether, an organometallic compound BB is formed. When compound BB reacts with ethanal, CH3CHO, a secondary alcohol cC is formed. The molecular structure of C6H11CI is given below. (1-klorometil)siklopentana, C6H11CI bertindak balas dengan akues natrium hidroksida, NaOH bagi menghasilkan satu alkohol primer AA. Apabila C6H11CI ditambah dengan magnesium, Mg dalam eter, sebatian organologam BB terbentuk. Apabila sebatian BB bertindak balas dengan etanal, CH3CHO, satu alkohol sekunder CC dihasilkan. Struktur molekul bagi C6H11CI diberikan di bawah. (1-chloromethyl)cyclopentanearrow_forwardAn unknown hydrocarbon Q has a formula C6H12. Q reacts with osmium tetroxide to give a diol R when oxidized with KMnQ4 in an acidic medium Q gives two products. One product is propanoic acid and the other is ketone S. Provide reaction equations to identify the possible structures of Q, R and S.arrow_forward
- 1.) Predict the reactants to produce the following compounds:arrow_forward(a) (i) 3-Methyl-2-butanol will react with sulphuric acid to give two isomeric alkenes in 3:1 proportions.(i) Write down the structures for these alkenes and assign appropriate systematic names to them. (ii) Name the most abundant isomer. (iii) Write down detailed mechanism for the formation of a minor product.arrow_forwardInterpret the acidity of alcohols on the basis of ground-state polarization and stability of the alcoholate anion(indicate and give symbols for bond polarization)! Compare the relative acidity of ethanol and 2-fluoroethanol!arrow_forward
- 7aarrow_forwardCompounds with more than one hydroxyl group can react with thionyl chloride differently from simple alcohols. In the reaction with thionyl chloride, the butane-1,2-diol gave a single organic product with 85% yield, according to the following balanced equation: (Suggest a reasonable structure for this product and make a mechanism to justify your reasoning using curved arrows to describe the motion of electrons)arrow_forwardfrom each. a) b) c) Predict the product of the following reactions. Provide the major organic product Br Br Br →→ Li CN acetone Na₂Sarrow_forward
- Identify (A) in the following reaction. 2H2 Pt (A) KMNO4 Warm conc. || С — С — о—н |CO,H + HO CO2H cis-cyclo hexane 1,2-dicarboxylic acid (a) (b) (c) (d)arrow_forwardEthanamine, CH,CH;NH2, is a weak base. pKa(CH;CH2NH3') = 10.6 (a) (i) Write an equation to show the reaction of ethanamine. CH;CH;NH2 with water. (ii) Explain, with reference to equation and the species in solution, what is mean be the terms weak and base.arrow_forwardThe compound below is treated with chlorine in the presence of light. CH2CH3 Draw the structure for the organic radical species produced by reaction of the compound with a chlorine atom. Assume reaction occurs at the weakest С-H bond.arrow_forward