Concept explainers
Interpretation:
The structural formulas for the expected products in the given reactions are to be identified.
Concept Introduction:
>The terpenes are the essential oils that are extracted from plants by gentle heating or steam distillation and have important hydrocarbon chemical. The terpenes having oxygen are called terpenoids and the monoterpene is made up of two or more 5-Carbon atoms named isoprene. The terpenes react with several reagents, chemicals, and catalysts like,
The pinenes are the oils obtained from pine trees.
>The alkaline potassium permanganate (
The
The number of moles of HCl used by 1 mol of terpene is equal to the number of double bonds present in the terpene.
>The caryophyllene undergoes addition with
The zingiberene undergoes catalytic hydrogenation with the help of hydrogen gas and platinum that act as catalysts to produce compounds of the order hexahydrozingiberene.
>The
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Organic Chemistry
- 1. Draw structures corresponding to the following IUPAC names: (a) 4-Methylpentanoic acid (b) o-Hydroxybenzoic acid (c) 2,2-Dimethylpropanoyl chloride (d) trans-2-Methylcyclohexanecarboxamide (e) p-Methylbenzoic anhydride (f) p-Bromobenzonitrilearrow_forwardDraw structures corresponding to the following names:(a) Octylamine (b) N-Methylpentylamine(c) N-Ethylaniline (d) 4-Aminobutan-2-olarrow_forwardCiprofloxacin is a member of the fluoroquinolone class of antibiotics.(a) Which of its rings are aromatic?arrow_forward
- Draw the structures of the following derivatives :(i) Propanone oxime (ii) Semicarbazone of CH3CHOarrow_forward(b) (i) The reaction between aromatic compound W, C,H$OC1 with an amine X, CH>N was carried out. The compound Y was extracted and purified from this reaction. It was then reduced by LİAIH4 followed by hydrolysis to obtain compound Z, which is a tertiary amine. Draw the structures for compounds W, X, Y and Z.arrow_forwardHydrocarbon A has the molecular formula C14H10C12. It absorbs eight molar equivalents of any hydrogen isotope using a Nickel catalyst. When subjected to ozonolysis, Compound A yields oxalic acid and the chiral chloropentane dioic acid. Write the reactions and propose a structure for A.arrow_forward
- A chemist synthesized compound X as a racemic mixture. When the ketone group in X was enzymatically reduced to the corresponding alcohol, a 100% yield was obtained of the product shown below. Choose the statement that best describes this result. ОН enzyme C;H1 `OCH,CH; pH 4.0 C3H1 `OCH,CH3 ОН ÕH X (racemic) (100% yield) One enantiomer of compound X reacts quickly with the enzyme. The other enantiomer of compound X is unreactive, but rapidly equilibrates with the reactive enantiomer under the reaction conditions. Since compound X was racemic, it makes sense that only a single product was obtained. O The product is a meso compound, so either enantiomer of compound X gives the same product. One enantiomer of compound X reacts quickly with the enzyme, while the other enantiomer of compound X remains unchanged.arrow_forwardWrite down the reaction of acetaldehyde with the following.(b) 2,4-dinitrophenylhydrazine (c) I2 / NaOHarrow_forward22). What is the major product of the following reactions? (A) (B) Br 1) NaCN 2) CH3MgBr 3) H30*/H₂O (C) LOH (D) CNarrow_forward
- On treatment with Cl2/hν, a compound with the formula C9H12 yields only a single monochloride. What is a possible structure of the compound?arrow_forwardComplete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →arrow_forward2. Draw the structure of the products that will be formed when aniline reacts with nitrous acid at 5 °C, followed by: (a) CUCN (b) CuBr (c) KI (d) (1) HBF4, (2) heat (е) НзРО4, Н-0 (f) Cu2O, Cu2*, H2Oarrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning