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- 3. Complete the chemical equations for the following reactions. Draw the structure (condensed structural formulas) for the dominant product and write the names of the reactants and products (organic compounds only.) d) CHy Name reactant: Name product: e) CH=C-CH + 2 HBr 4-Cて。 Name reactant: Name product:Draw out the structures (condensed structural formulas) for the following reactions (reactants and products) and name the product formed. a) Hydrohalogenation of 1,3-dimethylcyclopentene with HBr Name product: b) Hydrogenation of 3,4-dimethylcyclobutene Name product: c) Hydration of 3-ethyl-2-pentene cturslomeo Name product: d) Alkylation of benzene with 2-chloropropane (isopropylchloride) Name product: e) Mono-halogenation of 2,2-dimethylbutane with Cl2 Name product:1) The acid-catalyzed dehydration of 2-methyl-2-butanol yields two alkene products, what are the names of the two alkenes? 2) which of the two alkenes is the major product?
- 10) For the reaction between isopropyl 1-propyl (or 'n-propyl') ether and HBr, which type of reaction best matches the expected products? A) Acid-catalyzed dehydration B) Nucleophilic substitution reaction C) Ether cleavage reaction D) Nucleophilic addition-elimination reactionGive the reason for adding cyclohexane.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 inevery reaction.(Use condensed structural formula) (A) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr(B) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide(C) Formation of Gilman reagent using isopropyl bromide
- 1. Write in the correct reagents to accomplish these reactions. a) 2-methyl-2-pentanol b) CH3CH2CH₂OH → 2-chloro-2-methylpentane CH3CH₂CHa) Give the molecular formula and draw the skeletal structure for 3-bromo-3- methylhexane. b) Name (including E/Z stereochemistry) the FIVE alkenes that can produce 3-bromo-3- methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.??? c) Define the type of stereoisomerism present in 3-bromo-3-methylhexane. Name and draw the tetrahedral representation of the two stereoisomers?. d) For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile OH-): i) ii) iii) iv) State whether the reaction is likely to proceed by an SN1 or SN2 mechanism, and explain your choice Give the likely rate law for the reaction. Explain your choice. For the reaction intermediate, draw its structure and give the VSEPR description of the geometry at the reaction centre Give the names and draw the structures of the two reaction products. Explain your conclusions4-methyl-3-hexanol was prepared by reacting an alkene with either hydroboration-oxidation or oxymercuration-reduction. Draw the structure of the alkene that was used to prepare the alcohol in highest yield. • You do not have to consider stereochemistry. • Indicate the method of preparation by drawing either BH3 (for . If there is more than one alkene that can be used for a given method, draw all of them. If either hydroboration-oxidation or oxymercuration-reduction can be used, just give the structures for one method. Separate structures with + signs from the drop-down menu. ● 981 -- 26224 ? ChemDoodle Y hydroboration-oxidation), or Hg (for oxymercuration-reduction), in a separate sketcher. Sn [1
- The reduction of a certain alkene gave 2-methylbutane. It also gave acetic acid (CH3CO2H) as one of the products when treated with hot basic KMnO4 followed by acidification. Give the IUPAC name of this alkene.The condensed structural formula of an organic compound is CH3-CH2-CHBr-CHCl-CHCl-CHO. What is the name and type of this organic compound? 3-bromo-4,5-dichloro hexanal; aldehyde 4-bromo-2,3-dichloro hexanal; aldehyde 4-bromo-2,3-dichloro hexan-1-one; ketone 3-bromo-4,5-dichloro hexan-1-one; ketoneCompound L undergoes dehydrohalogenation to form hydrogen bromide and 1-methylcyclohexene. What is dehydrohalogenation? State the condition required for dehydrohalogenation. Draw the structural formula of compound L and name L.