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Q: Q#1 Give the IUPAC name for each compound. CI a. С. CI Br d. b. I,
A: The IUPAC names of above compounds are given in attached image.
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- Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3CH2 H3C CI CH3 CH3 CH3 T CHCIHow many isomers (structural, geometric, and stereo) have the formula C5H10, and have "cyclo" in their name? (i.e. they contain a ring) 4 06 07 5Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CIH2C CH2CI C=C H CH3CH2 CH3 C=C H3C CH3
- Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H3C CH3 CH3Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₂C CH3 C=C H3C-CH H₂C-CH3 CH3 CH3CH₂ CH3 H3C CH3a) 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 conclusions
- Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) Br. H C=C CH3 H₂C-CH₂ C=C H CHCH(CH3)2 CH3How many isomers (structural, geometric, and tereo) have the formula C5H10, and have "cyclo" in their name? (i.e. they contain a ring) 06 0 5 07 04 03Draw all 12 acyclic (no rings) isomers of formula C4H7Br. Include stereoisomers.
- 1. Name the following alkenes: H H CH3 CH2CH3 CH3 CH3CHCH2CH2CH H3C C=C H3C CH3 CH3 H2C=CHCHCH CH,CHẠCH2 CH3 H3C CH3 (b)Name the alkene below. Use ONLY E/Z designators to indicate stereochemistry. H H H3C CH3 CH;CH2CH2 CH31B. Provide the IUPAC name of the following compounds, with clear indication of stereochemistry for stereocenters and alkene. Me. (a) (b) (c) (d) Br "Ме CI