a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2,4-Dimethylhexa-1,4-diene with a mole of water
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Write a complete chemical equation showing reactants, products, and catalysts needed
(if any) for the following reaction and (2) Draw and name the organic compound found in
every reaction.(Use condensed structural formula)
(a) Complete hydrogenation of 2-Methylhexa-1,5-diene
(b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene
(c) Reaction of (4E)-2,4-Dimethylhexa-1,4-diene with a mole of water
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- (1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amideWrite a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction.(Use condensed structural formula) (A) Ozonolysis of 3,3-Dimethyloct-4-yne(B) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne(C) Partial hydrogenation using Lindlar’s Catalyst 2,2,5,5-Tetramethylhex-3-yneWrite a complete chemical equation showing reactants, products, and catalysts needed(if any) for the following reaction and (2) Draw and name the organic compound found inevery reaction. NOTE: USE CONDENSED STRUCTURAL FORMULA (A) Ozonolysis of 3,3-Dimethyloct-4-yne(B) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne(C) Partial hydrogenation using Lindlar’s Catalyst 2,2,5,5-Tetramethylhex-3-yne
- All about Alkene, Alkyne and Alkyl halides(1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (A) Ozonolysis of 3,3-Dimethyloct-4-yne(B) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne(C) Partial hydrogenation using Lindlar’s Catalyst 2,2,5,5-Tetramethylhex-3-yneUsing condensed structural formulas, write a balancedchemical equation for each of the following reactions:(a) hydrogenation of cyclohexene, (b) addition of H2O totrans-2-pentene using H2SO4 as a catalyst (two products),(c) reaction of 2-chloropropane with benzene in the presenceof AlCl3.Write balanced equations for the following reactions. Usestructural formulas to represent the organic compounds.(a) The complete combustion (to CO2 and H2O) of cyclopropanol(b) The reaction of isopropyl acetate with water to give acetic acid and isopropanol(c) The dehydration of ethanol to give ethene(d) The reaction of 1-iodobutane with water to give 1-butanol
- Draw complete structural diagrams of the following compounds. (a) 2-methyl,pent-2-ene (b) propyne (c) 2,3-dimethyl butane (d) cycloheptane(a) Alkenes are relatively stable compounds but are more reactive than alkanes and serve as a feedstock for the petrochemical industry because they can participate in a wide variety of reactions. Predict the products obtained from following reaction. Write the chemical reaction and name the products according to IUPAC system. (i) the reaction of 3-ethyl-3-methyl-1-pentene with hydrogen bromide (ii) the reaction of 3-ethyl-2-pentene with hydrogen bromide5. Give the structural formulae and name the functional groups of the following compounds. (a) 3-chlorobut-1-ene (b) butanedioic acid Name the functional group: (c) propanamide Name the functional group: (d) 3-methylbutanal Name the functional group: Name the functional group:
- What product is formed from the hydrogenation of2-methylpropene? (a) propane, (b) butane, (c) 2-methylbutane,(d) 2-methylpropane, (e) 2-methylpropyne.Name or write the condensed structural formula for the following compounds:(a) 4-methyl-2-pentene (b) cis-2,5-dimethyl-3-hexeneIndicate whether each statement is true or false. (a) Pentanehas a higher molar mass than hexane. (b) The longer the linearalkyl chain for straight-chain hydrocarbons, the higherthe boiling point. (c) The local geometry around the alkynegroup is linear. (d) Propane has two structural isomers.