Interpretation:
The number of the different monochloro derivative of
Concept introduction:
The free radical substitution reaction is the type of reaction that occurs by the free radical mechanism, free radical is formed during the reaction.
The chlorination of alkane is the radical substitution reaction. There are three steps are involved in the
The expression to calculate the mono chlorination product is as follows:
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General Chemistry: Principles and Modern Applications (11th Edition)
- 5) Limonene is a compound found in orange oil and lemon oil with molecular formula C₁0H16- When limonene is treated with 1 equivalent of mCPBA, the product is limonene oxide as depicted below. When limonene is treated with excess ozone (03) and then with dimethylsulfide (Me₂S), one of the organic products of the reaction is formaldehyde. Of the structures below, which correspond to the structure of limonene and/or the structure of the other major organic product when limonene is reacted with O3 and Me₂S? Please select any and all that apply. A) 'Н H B) ? H 1) 03 (XS) 2) Me₂S (xs) ? limonene, C10H16 D) mCPBA (1 equiv) E) limonene oxide None of the abovearrow_forwarda Give the chemical structure of (2R.3S)-2,3-dibromopentane b. Identify the following pairs of compounds as either enantiomers, diastercomers, or identical CN .COOH он CCH но CCH and NC COOH Give the structure of any reagent that can be used to enantiomerically resolve R- and S- ibuprofenarrow_forwardG.152.arrow_forward
- Alloocimene is a hydrocarbon found in turpentine. It has the molecular formula C₁0H16 and a UV absorption maximum at 290 nm. On hydrogenation with a palladium catalyst, 2,6-dimethyloctane is obtained. Ozonolysis of alloocimene, followed by treatment with zinc and acetic acid, produces the following four fragments: || CH3C-CH i O || || CH3CCH3 HC-CH Propose a structure for alloocimene. O || CH3CHarrow_forwardCompound X, C,4H12Br2, is optically inactive. On treatment with strong base, X gives hydrocarbon Y, C14H10: Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst to give z (C14H14) and reacts with ozone to give one product, benzoic acid (C,Hg02). Draw the structure of compound Z. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Ignore alkene stereochemistry. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. ChemDoodlearrow_forwardCompound A, C9H₁6 reacts with 1 molar equivalent(s) of hydrogen upon catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give: CHỊCHỊCH CH3CCH₂CH₂CH₂CH₂CH₂CCH3 || Propose a structure for A.arrow_forward
- Compound A has the formula C8H8. It reacts rapidly with KMN04 to give CO2 and a carboxylic acid, B (C7H602), but reacts with only 1 molar equivalent of H2 on catalytic hydrogenation over a palladium catalyst. On hydrogenation under conditions that reduce aromatic rings, 4, equivalents of H2 are taken up and hydrocarbon C (C8H16) is produced. What are the structures of A, B, and C. .CO.H COH A A B C OH A CO2H A B QUESTION 6arrow_forward1. There are several isomeric alkanes of molecular formula C6H14.Two of these exhibit the following 1H-NMR spectra. Propose a structure for each of the isomers. Isomer A: δ = 0.84 (d, 12 H), 1.39 (septet, 2H) ppm Isomer B: δ = 0.84 (t, 3 H), 0.86 (s, 9H), 1.22 (q, 2H) ppmarrow_forwardCompound A, C₂H16 reacts with 1 molar equivalent(s) of hydrogen on catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give: O CH3 O || CH3CCH₂CCH₂CCH3 CH3 Compound A Propose a structure for A. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.arrow_forward
- Compound C has the molecular formula C;H12. On catalytic hydrogenation, 1 mol of C absorbs 1 mol of hydrogen and yields a compound with the molecular formula C7H14. On ozonolysis and subsequent treatment with zinc and acetic acid, C yields only: The structure of C is:arrow_forward1. One version of canola oil is (C15H29CO2)3C3H5. (a) Write the transesterification chemical equation (similar to Eq. 12-7) for canola oil. (b) How much canola oil will be required to produce one ton of biodiesel? 2. Write the chemical reaction equations for hexene (C6H12), butanol (C4H9OH), and heptane (C7H₁6) for the Fischer-Tropsch synthesis process. If appropriate, the value of "n" must be used in a chemical equation.arrow_forwardBromine reacts with alkenes in methanol according to the equation: - When this reaction was carried out with 4-tert-butylcyclohexene, only one isomer was formed with the molecular formula C12H23BrO (80% yield). Which of the following is the structure more reasonable for this compound?. Explain your reasoning through acorresponding mechanism.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning