(a)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and
(b)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and functional group found at the end of the name. The second step is numbering of carbon skeleton in either direction. The third step is addition of substituents at appropriate carbon atoms.
(c)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and functional group found at the end of the name. The second step is numbering of carbon skeleton in either direction. The third step is addition of substituents at appropriate carbon atoms.
(d)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and functional group found at the end of the name. The second step is numbering of carbon skeleton in either direction. The third step is addition of substituents at appropriate carbon atoms.
(e)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and functional group found at the end of the name. The second step is numbering of carbon skeleton in either direction. The third step is addition of substituents at appropriate carbon atoms.
(f)
Interpretation: The structure corresponding to given name is to be drawn.
Concept introduction: One should follow the given three steps to derive the structure of the compound from its IUPAC name. The first step involves the identification of parent name and functional group found at the end of the name. The second step is numbering of carbon skeleton in either direction. The third step is addition of substituents at appropriate carbon atoms.
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ORGANIC CHEMISTRY
- Draw the correct structures for each name. а. (3R, 4R)-3,4-hexanediol b. meso-3,4-hexanediol c. There are several meso structures for 2,3,4-trichlorohexane. Draw two of them.arrow_forwardBr KOH / DMSO 6. b. 2-methyl-1-propanol d. 1,2- a. 2-methylpropene propanediene c. no reaction e. something else! 7. cyclopentanol + NaH + DMSO+ bromopropane à(major product) a. cyclopentene reaction b. propene c. propyl cyclopentyl ether d. no e. something else!! 8. 2-bromo-3-methylbutane + KOH / DMSO à(major product) a. 2-methyl-1-butene d. no reaction b. 2-methyl-2-butene c. 3-methyl-2-butanol e. something else!! 9. 2-chloro-3-methylbutane + KI / DMSO à(major product) a. 2-methyl-1-butene b. 2-methyl-2-butene c. 3-methyl-2-iodobutane d. no rxn e. something else!! 10. (S)-2-iodobutane + NaN; / DMF à (major product) N3 c. f. something else!! а. b. с. d. е. no rxn 11. cyclohexene + NBS/ CCl, / light followed by K* t-butoxide / t-butanol with heating à a. cyclohexene b. 1,3-cyclohexadiene cyclohexane e. something else! c. 1,2-cyclohexadiene d.arrow_forwardReagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).arrow_forward
- What reagent (reactant) could be used to produce the product above from 1-butene? A. HBr B. Br2 C. OBR D. more than one of the above is correctarrow_forwarda. What alkane, with molecular formula C5H12, forms only one monochlorinated product when it is heated with Cl2? b. What alkane, with molecular formula C7H16, forms seven monochlorinated products (disregarding stereoisomers) when heated with Cl2?arrow_forward1. What is it's type of reaction (Sn1, Sn2, E1, E2, Nucleophilic Addition, Nucleophilic Acyl Substition or Redox reaction). 2.What is it's major product.arrow_forward
- 4. Syn and anti addition can occur with alkenes. 1. Describe syn and anti addition. b. Give an example of syn addition to an alkene and explain why it is syn. c. Give an example of anti addition to an alkene and explain why it is anti. 5. The following reactions shows the dehydration of 2-methylcyclohexanol. Why is 1-methylcyclohexene the major product? X OH H3PO4 84% 16%arrow_forward51. What is the product of the reaction below? 1. BD, THF 2. H,O,/OH" OH он он B D 52. Provide the proper IUPAC name for the alkene shown below. a. (S)-3-ethyl-3-methylcyclohexene b. (R)-3-ethyl-3-methylcyclohexene c. (S)-3-ethyl-3-methylcyclohexane b. (R)-3-ethyl-3-methylcyclohexane 53. Which is the product for the following E2 reaction? smbns NaOCH, Ph E2 CI CI Ph CI Ph Ph To mainedom Ph vlovalton CI C D 44What is 54. Provide the reagents for the transformation of cyclopentane to cyclopentene. a. (1) Br2, hv; (2) NaOH; b. (1) Br2, hv; (2) HCl; c. (1) HCI, (2) Br2, hv; d. (1) Br2, hv; (2) H2O 55. Which intermediate is not involved in the mechanism of the reaction below? OH H,SO, HOH C 10arrow_forward1. What would be the major product in the given reaction? 1) 9-BBN 2) H,О2, NaOH, Н,о a. 2-Phenylethanal b. 1-Phenylethanol c. Ethylbenzene d. Acetophenone 2. What would be the product for the following reaction? `NH2 HO. OH но а. b. С. d.arrow_forward
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