Concept explainers
(a)
Interpretation: The products formed by the Friedel-Craft alkylation of given compound with
Concept introduction: The replacement or substitution of one
(b)
Interpretation: The products formed by the Friedel-Craft alkylation of given compound with
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.
(c)
Interpretation: The products formed by the Friedel-Craft alkylation of given compound with
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.
(d)
Interpretation: The products formed by the Friedel-Craft alkylation of given compound with
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron deficient chemical species that contains positive charge are known as electrophile. In electrophilic aromatic substitution reaction, electrophile takes the position of hydrogen atom by attacking the electron rich carbon atom of benzene.
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ORGANIC CHEMISTRY W/ALEKS
- What Wittig reagent and carbonyl compound are needed to prepare each alkene? When two routes are possible, indicate which route, if any, is preferred.arrow_forwardwhich of the following is product of this reaction?arrow_forwardDraw 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.arrow_forward
- Draw the organic product(s) formed when CH3CH₂CH₂OH is treated with each reagent. a. H₂SO4 d. HBr g. TsCl, pyridine b. NaH h. [1] NaH; [2] CH₂CH₂Br e. SOCI₂, pyridine f. PBr3 c. HCI + ZnCl₂ Hint: NaH deprotonates the alcohol forming an alkoxidearrow_forwardDraw the product formed when each organometallic reagent is treated with H2O.arrow_forwardDraw the product formed when C6H5N2 +Cl− reacts with each compound.arrow_forward
- Draw the products formed from LiAlH4 reduction of each compound.arrow_forwardSynthesize each compound from cyclohexanone and organic halides having s4 C's. You may use any other inorganic reagents. OCH3 a. C. OH b. d.arrow_forward5. What reagents are needed to convert toluene (C,H,CH,) to each compound? a. C.H.COOH b. C.H₂CH₂Br c. p-bromotoluene d. o-nitrotoluene e. p-ethyltoluene f.arrow_forward
- Draw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridinearrow_forwardLabel each compound as more or less reactive than benzene in electrophilic aromatic substitution.arrow_forwardFor each of the following alkenes, draw the structure of two different alkyl halides that yield the given alkene as the only product of dehydrohalogenation.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning