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- 7. Name the following phenols. b) OH c) d) a) OH Br- HO CI Br 8. Name the following ethers. b) a) CHy-0-CH-CHy CH-0-CH3 c) d) Cゅ-C-o10) 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 reactionDraw 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:
- what should be the preferred product in the following reaction? CH₂ Som OH CH3 CH3 § § a) b) a H₂SO A C CH₂ c) ? CH3 d)4) Complete each reaction and name the product w (CH3)2C=CHCH3 2-methyl-2-butene HCI Br₂ H₂O/acid i) BH3 ii) H₂O₂ & base Ozone, O37. Reaction product of 3-methyl-butene with hydrochloric acid:a) 2-methyl-3-chlorobutaneb) 3-methyl-3-chlorobutanec) 2-chloro-3-methyl butaned) 2-chloro-2-methyl butane 8. What type of reaction takes place when CO2 + H2O and energy are obtained from 3-methyl butyne?a) Hydrogenationb) Halogenationc) Partial oxidationd) Total oxidation
- 10. Consider the hydrogenation reaction of compound X to Y: H₂, Pt X (C8H14) →Y (C8H16) 25°C One can conclude that X has: A) no rings and no double bonds. B) no rings and one double bond. C) one ring and one double bond. D) two rings and no double bonds. E) one triple bond.The IUPAC name is: HO a) l,,4-trimethylcyclohexano) b) I,4,4 - trimethyl cyclohexanol C) 3,3,6-te?methyl cyclohexano) d) 2,5,5-trimethylayclohexano) The IUPAC name 9s: OH Br a) 6-bromo-2-methylcyclohew-1-en-3-01 b) 4 -bromo- a- methylycohen-2-en -\-0l C) S-bromo -1-methyicgclohex-l- en-2-01 d) 3-bromo-l-methylcyclohex-1-en-6-01 e) s-bromo-2-methylcyclohexol- en -2-017. Draw the condensed structural formula of the product for each reaction. Name the reactant and the product. 아 HS OH 140°C or th lall 180 Ho CH CH3 CHy-CH -CH-CH + PE CH3
- Identify the product, if any, that would form in each of the following reactions. 73) CH3 - CH2-CH2-OH [0] A) || CH3- CH2 - C- CH3 74) [0] B) CH 3 - CH 2 - CH -OH || CH3 CH3 - CH2 - CH Match the structural formula with the correct functional group. 75) CНз - СH2 -ОН A) alcohol 76) CH3 – CH2¤0 ICH3 B) thiol 77) CH3- CH2 - SH C) ether Select the correct name for the following. 78) CH3 - CH2 - CH2 - SH A) propanethiol 79) CH3 - CH2 - O - CH2 - CH3 B) diethyl ether 80) C) m-ethylphenol OH CH2CH3 D) 1-ethyl-3- hydroxycyclohexene E) propane sulfide10) Synthesis: Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. ♡ Br Br3. 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 H2