Interpretation:
The nature of the compound formed and the type of reactioninvolved need to be described with given molecular formula.
Concept introduction:
Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.
Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.
Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a functional group is substituted by any other functional group is called substitution reaction.
Elimination reaction: A reaction in which two substituent groups are detached and a double bond is formed is called elimination reaction.
Addition reaction: It is the reaction in which unsaturated bonds are converted to saturated molecules by the addition of molecules.
The reaction in which hydrogen is added to the compound in the presence of catalyst is known as hydrogenation.
The number of moles of hydrogen absorbed will be equal to the number of double bonds.
The reaction in which a halide group is removed to form an
This reaction in which
Piperonal is an acetal, which has an
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Chapter 16 Solutions
Organic Chemistry
- In the chemical synthesis of DNA and RNA, hydroxyl groups are normally converted to triphenylmethyl (trityl) ethers to protect the hydroxyl group from reaction with other reagents. Triphenylmethyl ethers are stable to aqueous base but are rapidly cleaved in aqueous acid. (a) Why are triphenylmethyl ethers so readily hydrolyzed by aqueous acid? (b) How might the structure of the triphenylmethyl group be modified to increase or decrease its acid sensitivity?arrow_forwardRecalling the reactions of alcohols from Chapter 10, show how to synthesize each compound from an organohalogen compound and an oxirane, followed by a transformation of the resulting hydroxyl group to the desired oxygen-containing functional group.arrow_forwardGive the products formed when benzaldehyde and benzoic acid are treated with the given reagents. h. 2 moles CH3OH, H+i. CH3MgCl, then H2O, H+j. H2Oarrow_forward
- 4. Heptyl phenyl ketone was formed from the Friedel-Crafts acylation of benzene with an acyl chloride. What is the IUPAC name of the original acyl chloride? 5. How many isomers are there Of C6H14? 6. Aside from a halogenated alkane, what other product results from the bromination of hexane? Write the formulaarrow_forwardMethyl benzoate was exposed to a nitration test, although it was difficult to see the formation of a fragrant yellow solution. What produced this consequence?arrow_forwardIn an advanced synthetic chemistry experiment, a researcher prepares a compound, ZY-7, by reacting a ketone (C5H10O) with hydroxylamine (NH2OH), followed by heating in the presence of an acid catalyst. The resulting compound, ZY-7, is then treated with a solution of sodium nitrite (NaNO2) and hydrochloric acid (HCl) at low temperature. Identify the class of compound that ZY-7 most likely belongs to after this series of reactions." A) Amide B) Oxime C) Nitro compound D) Diazonium salt E) Ester Don't use chatgpt please provide valuable answerarrow_forward
- Compound H with molecular formula C6H12O showed no reaction in chromic acid test. Compound H undergo dehydration reaction to produce compound I. Compound J is produced when compound I react with HBr. Reaction of compound J with methanol produced compound K and I. Draw the structure of H, I, J, and K.arrow_forwardThe reaction of p-cresol with CH2=O resembles the reaction of phenol (PhOH) with CH2=O, except that the resulting polymer is thermoplastic but not thermosetting. Draw the structure of the polymer formed, and explain why the properties of these two polymers are so different.arrow_forwardWrite reactions of aniline with the following reagents: a. CH3COCl b. Br2 c. CH3Iarrow_forward
- Provide the reagents necessary to complete the following reactions.arrow_forwardFrom the given two compounds in the image, which reagents would differentiate the pair? a. Br2 in CH2Cl2 b. CrO3, H2SO4, acetone c. concentrated HCl with ZnCl2 d. aqueous FeCl3 e. aqueous NAHCO3 f. ammoniacal AgNo3arrow_forwardAn unknown hydrocarbon A with the formula C6H10 reacts with 1 molar equivalent of H2 over a palladium catalyst to give B C6H12 (Rxn 1). Hydrocarbon A also reacts with OsO4 to give the glycol C (Rxn 2). A gives 5-oxohexanal on ozonolysis (Rxn 3). Draw the structures of A, B, and C. Give the reactions.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning