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- Explain why the reaction in Problem 18.48 proceeds dramatically more slowly under neutral conditions than under either acidic or basic conditions.1) Draw the structure of the alkene product for the E2 elimination reaction shown below. 1)a 2)b 3)c 4)d 5)ec) 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:
- The pictured reaction shows an alkyl bromide being converted into an alkene. Choose all reagents that would produce the pictured alkene as the major product. A) NaOH/H2O B) H2O C) tBuOK/tBuOH D) EtONa/EtOHExplain why ethene does not react with HX ( X=Cl , Br or I) under normal conditions.Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہ
- what will be the type of interaction of ethane with bromine: a) radicals b) ionic c) nucleophilic d) electrophilicSynthesize each compound from (CH3)3CH.Draw the products formed when each compound is treated with HNO3 and H2SO4.State whether the reaction occurs faster or slower than a similar reaction with benzene.
- Draw the organic products formed when cyclopentene is treated withfollowing reagent. [1] CH3CO3H; [2] H2O, HO−Select the correct product for the following reaction.Match each reagent to the product that it forms. Multiple reagents may form the same product. HO Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It eft ft D) E) F) "got soft soft MSO MsO CI