Concept explainers
Interpretation: Order of stability within allylic or benzylic carbocation boxed in below figure has to be explained.
Concept introduction: Organic compounds are covalent in nature that undergoes a reaction by heterolytic cleavage or homolytic cleavage.
In heterolytic cleavage, shared pair of electrons is taken away by one of the atoms which result in charged species. In homolytic cleavage, shared pair of electrons are equally distributed between two atom that results in free radicals.
Carbocation is a general term employed for a postively charged carbon irrespective of valency of carbon. In carbocation, carbon is bonded to 3 atoms or groups and has only sextet of electrons so it behaves as an electron-deficient species. It is
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Organic Chemistry: A Guided Inquiry
- Indicate the correct option.a) Isopolianions are formed around metallic atoms in a low oxidation stateb) Non-metals such as N, S, C, Cl... give rise to polyacids (oxygenated).c) Both answers are false.arrow_forwardplease show major prodcut and stereochemarrow_forwardIndicate the correct option.a) The most frequent coordination structure of isopolianions is the prismb) Heteropolianions incorporate alkaline cations into their structuresc) Both answers are falsearrow_forward
- Indicate the correct option. Isopolyacidsa) are formed by polymerization of oxoanions of metals of groups 5-7 in their highest oxidation states.b) are formed by polymerization of oxoanions of metals of groups 5-7 in their lowest oxidation states.c) are formed by polymerization of oxoanions of metals of groups 8-9 in their lowest oxidation states.d) are heteropolyacids that contain a non-metallic element inside.arrow_forwardOrgan Classifying organic reactions The following chemical equation is for an elimination reaction, where the important atoms, groups, and bonds involved have been highlighted for you: HO H H* + H-OH H Use the information provided to predict the missing organic product and draw its structure in the drawing area below. Make sure to use the same skeletal ("line") style for the structure as the rest of the equation. Explanation Check Click and drag to start drawing a structure. C + 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardSome could be more than one answerarrow_forward
- Draw the simplest mechanism possible for the reaction. You may need to redraw structures to show bond lines or lone pairsarrow_forwardshwo major product and stereochemarrow_forwardQuestion 8 Which of the following is the correct mechanism for the elimination reaction of 2-bromo-2,3- dimethylbutane with methoxide? .. OCH Br Br OCH e POCH OCHarrow_forward
- Classify each of the following organic reactions in the table belowarrow_forwardIndicate the relationship between isopolianions and isopolimetalates.arrow_forwardKetenes are highly reactive carbonyl compounds that easily hydrolyze to give carboxylic acids, orsolvolyze (e.g., with methanol) to give methyl esters (Equation 1). Consider the methanolysis of thesubstituted ketene shown below (Equation 2). The methyl ester is formed as expected, but the epoxideundergoes a rearrangement to give the unsaturated alcohol product. Draw the structures for each step of this process (use the pushing electron method to show how each step occurs). include lone pairs - start with the methanol oxygen lone pair attacking the carbonylcarbon of the ketene.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning