Problem 1. Show how 1-methyl-1-isoproproxycyclopentane may be synthesize by: a) William ether synthesis b) Acid-catalyzed Addition of Alcohol to Alkenes
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- c) Classify the reaction below as an oxidation, a reduction, or neither.cis-pent-2-ene → pentaneA) oxidationB) reductionC) neitherAnswer: 2) Which of the following compounds has carbon in the highest oxidation state?A) CO2B) CH3COCH3C) CH3CH2OHD) CH3C(OCH2CH3)3Answer: 3) Which of the following reagents is the best choice for oxidizing a primary alcohol toan aldehyde?A) H2CrO4B) pyridinium chlorochromateC) Na2Cr2O7, H2SO4D) KMnO4E) LiAlH4Answer:Show how to prepare compound from 1-heptene. Q) 1,2-Dichloroheptaneh) Draw a stepwise mechanism for the following reaction. OH NH,OH МеОн Suggest two methods to synthesize the alkene helow from cyclonentanone it
- 1) Provide the name for each structure shown. NO ₂ 2) Draw the structure of the molecule with the following name: a) (1R, 3S)-Cyclopent-4-ene-1,3-diol b) (2R, 3Z)-3-Chloro-2phenylhex-3-enal c) (2E,4Z)-Hepta-2,4,6-trienoic acid d) (3R, 4E)-3-isopropyl-6-oxohex-4-enenitrile H₂C NH CH3 CH3 H₂N CH3Draw the following compoundsDraw reaction mechanisms with all reactants, arrows, intermediates, and products. Your mechanism must account for all the products if more than one product is formed. 4-methycyclohexanol with phosphoric acid H3PO4 to for 1-methycyclohexene, 3- methylcyclohexene and 4-methycyclohexene
- QuestionVShow how you would convert 2-methylcyclopentanol to the following products. Any of these products may be used as thereactant in any subsequent part of this problem.(a) 1-methylcyclopenteneTo synthesize the following substances using any alkene as a starting material. Name the starting material.