(a)
To determine: The structure of the substitution product that is obtained by the reaction of
Interpretation: The structure of the substitution product that is obtained by the reaction of
Concept introduction: The replacement or substitution of one
(b)
To determine: The structure of the substitution product that is obtained by the reaction of
Interpretation: The structure of the substitution product that is obtained by the reaction of
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. There are two types of substitution reaction. First one is electrophilic substitution reaction in which electrophile is present as a reagent and second one is nucleophilic substitution reaction in which nucleophile is present as a reagent.
(c)
To determine: The structure of the substitution product that is obtained by the reaction of
Interpretation: The structure of the substitution product that is obtained by the reaction of
Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. There are two types of substitution reaction. First one is electrophilic substitution reaction in which electrophile is present as a reagent and second one is nucleophilic substitution reaction in which nucleophile is present as a reagent.
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Organic Chemistry (9th Edition)
- Synthesize each compound from benzonitrile (C6H5CN) as the only organic starting material; that is, every carbon in the product must originate in benzonitrile.arrow_forwardpyridine reacts with 1-bromobutane to give?arrow_forwardThe synthesis of cyclohexanone oxime from cyclohexanone is a net? a. elimination b. substitution C. addition d. rearrangement The synthesis of cyclohexanone oxime from cyclohexanone is a net of carbon? a. reduction b. oxidation C. not a redox of carbon Balancing the equation of all the starting reagents going to final products in the synthesis of cyclohexanone oxime from cyclohexanone (see the first question), what is the coefficient of water if the coefficient of cyclohexanone is one? Give your answer in decimal form with no units. Answer: Select all the effects that you should see in an infrared going from cyclohexanone to cyclohexanone oxime. Selecting wrong answers may give you a negative score. a. a peak should disappear from above 3000 cm -1 b. a new peak should appear above 3000 cm -1 c. the frequency of the infrared absorption should go down in the double bond region d. the frequency of the infrared absorption should go up in the double bond regionarrow_forward
- 19. Write a series of equations to illustrate the synthesis of 3-pentanone from an alkene (you must choose the correct alkene compound to begin your series of reactions). Include the names and structures of all reactants and products. (3T/I, 3C)arrow_forwardDraw the products formed when p-methylaniline (p-CH3C6H4NH2) is treated with each reagent. a. HCl b. CH3COCl c. (CH3CO)2O d. excess CH3I e. (CH3)2C = O f. CH3COCl, AlCl3 g. CH3CO2H h. NaNO2, HCl i. Part (b), then CH3COCl, AlCl j. CH3CHO, NaBH3CNarrow_forwardThe reaction of 4-methylcyclohexanone with CH3MgBr followed by neutralization gives two alcohols. These two alcohols are A. enantiomers formed in equal amounts. B. diastereomers. C. constitutional isomers. D. enantiomers formed in unequal amounts.arrow_forward
- Oxidation of 1-butanol and 2-butanol yields (respectively) a. butanal exclusively b. 2-butanone exclusively c. butanal and 2-butanone d. butanal and 2-butanone if PCC is the oxidizing agent e. butanal and 2-butanone if the Jones reagent is the oxidizing agentarrow_forward. Which of the following can be both formed from bromoethane and converted directly into ethanal? CH3CH2Br → X → CH3CHO a. CH3CH2OH b. CH3OCH3 c. CH3COOH d. H2C=CHBrarrow_forwardUsing 4-bromotoluene as starting material, make a. 4-bromobenzoic acid b. 4-methylbenzoic acid c. P-bromophenylethanoic acid: Br OHarrow_forward
- C. Draw a structural formula for the principal organic product formed when each compound is treated with K2CrzOr/H2SO4 if there is no reaction, say so. 1. butanal 2. benzaldehyde 3. cyclohexanone 4. cyclohexanol 5. 2-pentanonearrow_forwarda. Draw the structures and give the common and systematic names for alkynes with molecular formula C7H12. Ignore stereosiomers. (Hint: There are 14.) b. How many would there be if stereoisomers are included?arrow_forwardname and draw the product/s formed from the reaction of 3-methylpent-2-ene: 1. with HBr 2. with Cl2 3. H2O in the presence of H2SO4 4. ethanol in the presence of H2SO4 5. Br2, H2O 6. [1] 9-BBN; [2] H2O2, OH-arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning