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- 5. For each of the following pairs, circle the most stable alkene and provide the name for each of them. X VS. 2.0 VS. VS.8. What is the IUPAC name of CHCH, CH, CH3-CH-O-CH, CH; Da. 1-ethoxy-1-methylbutane Ob. 2-ethoxypentane O c. 1-methoxyhexane Od. 2-ethoxy-2-n-propylethane4. Draw the following compounds a. 1-chloro-4-ethyl-3-methylnonane [ Gatusofom gnit b. 4-methyl-2-pentyne Job i anticas) enod totall xbacd bigin i emoczopertori c. 1-bromo3-methylbutane d. 4-ethyl-3-fluoro-1-hexene
- Name the following alkyne. Be sure to use hyphens (-) not endashes (-). CI-Give the systematic name of the alkene, indicating cis or trans configuration. .CH3 H. CH3 systematic name: Draw trans-2-hexene. Include all hydrogen atoms. Select Draw Rings More Erase HWhich structure is trans-3-hexene? CH3. H CH3, H OCH3CH₂ H OCH3CH₂ H C. C. FC. C H CH₂CH₂CH3 CH₂CH₂CH3 H H CH₂CH3 CH₂CH3 H
- How many moles of Bra are required to completely halogenate the alkene?A. One moleB. Two molesC. Three molesD. Four moles What is the expected arrangement of the bromine atoms relative to each other amongthe carbon involved in pi bonding?A. anti-conformationB. syn-conformationC. trans-configurationD. cis-configuration What happens to bromine when it is adjacent to an alkene during a chemical reaction?A. Bromine becomes stable. (? kasi before brown siya/acidic tas naging colorless? Jk ewan)B. Bromine becomes polarized.C. Bromine becomes hybridized.D. Bromine becomes acidic. The relative arrangement of bromine atoms in the product is primarily due to:A. ElectronegativityB. RepulsionC. Hydrogen bondingD. Atomic weightWhat is your observation after the reaction?A. A yellow flame is produced.B. Bromine water decolorizes.C. The alkene becomes denser.D. A brown precipitate forms.Name the alkyne. Spelling and punctuation count. H3C-CH2-CH2-CH-CCH CH2 CH, name:3. Which carbon would the Br of HBr add to in the following unsymmetrical alkenes? 1 Problem Set #7 Chemistry 227 а. b. С. d. H3C H3C е. H Н. H3C. TH. CH3 H H H the C=C in the ring do not react with H*