Interpretation:
The listed nucleophiles, in the order from the slowest
Concept introduction:
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Chapter 9 Solutions
Organic Chemistry: Principles And Mechanisms
- 4. ) Rank the nucleophiles from weakest to strongest. (1 = weakest, 3 = strongest) %3D HO,arrow_forward5. For the following pairs of species, which is the strongest nucleophile in acetone? Explain. By ü) yarrow_forwardYour answer is incorrect. Predict the relative rates of these reactions. That is, select 1 next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. Incorrect Your answer is incorrect. Predict the relative rates of these reactions. That is, select I next to the reaction with the fastest rate, 2 next to the reaction with the next fastest rate, and so on. Note for advanced students: you may assume these reactions all take place in a polar aprotic solvent, like DMSO. Reaction Relative Rate G + H₂O - OH₂ 2 Br + H₂S - + Br 3 + H₂S SHI + ci I (fastest) Br + H₂O OM₂ + Br 4 (slowest)arrow_forward
- Identify the strongest nucleophile. HO™ O NaSH OCH3CH₂OCH2CH3 Orarrow_forwardIn an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.arrow_forwardRank the nucleophiles in following group in order of increasing nucleophilicity. −OH, Br−, F− (polar aprotic solvent)arrow_forward
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENTOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning