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Is the organic reactant oxidized, reduced, or neither in each of the following reactions?

Short Answer

Expert verified

Both the reactants in the reactions given are oxidized.

Step by step solution

01

Introduction

In the case of organic compounds, what is meant by oxidation-reduction, is the change in the number of carbon-heteroatom bonds and carbon-hydrogen bonds. By calculating the difference in the number of carbon-heteroatom bonds of reactant and product or by calculating the difference in the number of carbon-hydrogen bonds in the reactant and product, it can be found whether the reactant has been oxidized or reduced.

If the number of carbon-heteroatom bonds increases and the number of the carbon-hydrogen bond decreases in going from reactants to products, the reactant is said to be oxidized. This is because when carbon makes a bond with a more electronegative heteroatom, its electron density is decreased, and thus oxidation occurs.

On the other hand, If the number of carbon-heteroatom bonds decreases or the number of the carbon-hydrogen bonds increases in going from reactants to products, the reactant is said to be reduced. This is because, when carbon makes a bond with hydrogen, it gains electron density, so it is said to be reduced.

02

Explanation a)

In the given reaction, 2-hexene is giving 2,3-duhydroxyhexane, which is oxidation, as there are 12 C-H bonds in 2-hexene but 2 C-OH bonds in the product 2,3-dihydroxyhexane.i.e., the number of C-O bonds is increasing.

03

Explanation b)

In the given reaction, cyclohexane is giving benzene, which is oxidation, as there are 12 C-H bonds in cyclohexane while 6 C-H bonds. i.e., the number of C-H bonds is decreasing.

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Most popular questions from this chapter

Silicon lies just below carbon in Group 4A (14) and also forms four covalent bonds. Why arenโ€™t there as many silicon compounds as carbon compounds?

Among alkenes, alkynes and aromatic hydrocarbons, only alkenes exhibit cis-trans isomerism. Why donโ€™t the others?

What is the range of oxidation states for carbon? Name a compound in which carbon has its highest oxidation state and one in which it has its lowest.

Some of the most useful compounds for organic synthesis are Grignard reagents (general formula , where X is a halogen), which are made by combining an alkyl halide, , with. They are used to change the carbon skeleton of a starting carbonyl compound in a reaction similar to that with :

(a) What is the product, after a final step with water, of the reaction between ethanal and the Grignard reagent of bromobenzene?

(b) What is the product, after a final step with water, of the reaction between 2-butanone and the Grignard reagent of 2-bromopropane?

(c) There are often two (or more) combinations of Grignard reagent and carbonyl compound that will give the same product. Choose another pair of reactants to give the product in (a).

(d) What ยฑOH group at the end of the carbon chain?

(e) What Grignard carbonyl compound must react with a Grignard reagent to yield a product with the reagent and carbonyl compound would you use to prepare 2-methyl-2-butanol?

Define each type of isomer: (a) constitutional; (b) geometric; (c) optical. Which types of isomers are stereoisomers?

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