Concept explainers
(a)
Interpretation: The stronger nucleophile out of
Concept introduction: Solvent is required to dissolve the starting material in it. The substitution reaction involves polar starting reactant which is soluble in polar solvent. A solvent in which hydrogen atom is bonded to electronegative
(b)
Interpretation: The stronger nucleophile out of
Concept introduction: Solvent is required to dissolve the starting material in it. The substitution reaction involves polar starting reactant which is soluble in polar solvent. A solvent in which hydrogen atom is bonded to electronegative
(c)
Interpretation: The stronger nucleophile out of
Concept introduction: Solvent is required to dissolve the starting material in it. The substitution reaction involves polar starting reactant which is soluble in polar solvent. A solvent in which hydrogen atom is bonded to electronegative
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Organic Chemistry
- Rank the nucleophiles in each group in order of increasing nucleophilicity. a.−OH, −NH2, H2O b.−OH, Br−, F− (polar aprotic solvent) c.H2O, −OH, CH3CO2−arrow_forwardWhich is best nucleophile?arrow_forwardIdentify the stronger nucleophile in the following pair of anions. HO− or Cl− in a polar aprotic solventarrow_forward
- Which of the following molecules is most nucleophilic? OA. NaOCH₂CH3 OB. CH3CH₂OH OC. NaOC6H5 OD. C₂H5OH 1 E.CH3COONaarrow_forward10. Which species is acting as the nucleophile in this reaction? а. Н b. CE c. The carbocation cr d. The pi bondarrow_forwardDraw the nucleophile and electrophile precursor for each structure.arrow_forward
- HCOO- > HO- > (CH3)2 Sort from best nucleophile to worst nucleophilearrow_forwardDraw the product of nucleophilic substitution with each neutral nucleophile. When the initial substitution product can lose a proton to form a neutral product, draw the product after proton transfer.arrow_forward10. Consider the below reaction between the acetylide ion and methanol. Draw the conjugate acid that is formed as a product in this reaction.arrow_forward
- Q6arrow_forwardOptions for each: blank 1: A B blank 2: it has a better leaving group it is a polar aprotic solvent it has a stronger nucleophile blank 3: A B blank 4: it forms a more stable carbocation it has a better solvent it has a better leaving group blank 5: A B blank 6: it has a better solvent it has a better leaving group it has a stronger nucleophilearrow_forwardIs this a good or a bad nucleophile?arrow_forward
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