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- What reagents are needed to convert 1-ethylcyclohexene into (a) 1-bromo-2ethylcyclohexane; (b) 1-bromo-1-ethylcyclohexane; (c) 1,2-dibromo-1-ethylcyclohexane?N|ON|OU|G fic|Gb| app.101edu.co Maps YouTube 0³ A ℗ 2 F2 W S CO X G d B 2|GD|QC|GA Question 13 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 1- 3- 2- 6- 4- 5- iso tert- di tri sec- cyclo pent hept non 99 MacBook Air # 3 > 0 80 F3 E D $ S4 Aav F4 R F 0, % 5 F F5 T G 6 Y & 7 H F7 U * 00 8 J DII F8 W G 1 CS UONEE 9 K F9 ) O O F10 L Done P Gri J F11 + (What are the starting reactants for the following reaction? 4 X = cyclohexa-1,3-diene; Y = ethyl acrylate X = cyclopenta-1,3-diene; Y = acrylaldehyde X = cyclohexa-1,3-ene; Y = ethyl acrylate X = hexa-1,3-diene; Y = ethyl propiolate CO₂C₂H5
- How many alkenes or cycloalkenes with the general formula C9H16 can you treat with HCl to obtain 1-chloro-1-ethyl-3,4-dimethylcyclopentane as a major product?The name of this compound. Br H. C=C Cl F O Z-2-bromo-2-chloro-1-fluoroethene E-1-bromo-1-chloro-2-fluoroethene O cis-2-bromo-2-chloro-1-fluoroethene trans-1-bromo-1-chloro-2-fluoroethene These compounds possessed strong and characteristic odors. O Alkynes Alkenes O Alkanes ArenesAssuming nucleophilic substitution reactions will occur, which will produce racemic products? CH;CH,CH(CI)CH3 + NANH, CH3CH2CH(CI) CH3 + CH3S¯Na* CH;CH,CH(CI)CH,CH3 + NH3 O CH;CH2CH(CI) CH3 + CH3OH
- Name the alkenes below. Use ONLY E/Z designators to indicate stereochemistry. H3C H Ja H CH₂-C H CH3 CH₂CH3Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.Name the alkene below. Use ONLY E/Z designators to indicate stereochemistry. H CH3 H3C C=C H2C=CHCHÇH H ČH3
- Classify the follow halide as vinyl, allyl, aryl, benzyl, vicinal or geminal. ✪ geminal vicinal vinyl O allyl aryl benzyl Br H Cl HThe two alkenes below react with HI at different rates. CH3CH=CHCH3 and CH₂=CH₂ Draw the structural formula of the MAJOR product formed by the alkene having the HIGHER reaction rate. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. TAYY [ ] در ChemDoodle ⓇFrom : cis (1s, 4s) -1-bromo- (tert-butyl) cyclohexane trans (1r, 4r)- 1- iodo- 4- isoproppylcyclohexane 1,5 - dimethylcyclohex -1 -ene trans (1r, 4r)- (tert - butyl) - 4- fluorocyclohexane trans (1r, 4r) - 1- bromo - 4- (tert - butyl) cyclohexane 1,3,5 - trimethylcyclohex - 1- ene . 5- Choose the substrate from the ones that drawn and illustrate an example complete Markovnikov addition mechanism using the reagents of your choice showing all stereochemical consequences. Identify if your addition mechanism is syn addition or anti addiction (Use curved arrows to show the electron movement in everyday steps). use ChemDraw if possible..