Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
Question
Book Icon
Chapter 10, Problem 1LGP
Interpretation Introduction

Interpretation:

The structures for all the organic products that would result when excess of cis1,3dimethylcyclohexane and cis1,2dimethylcyclohexane react with Br2 and Cl2 are to be drawn.

Concept Introduction:

The compounds that have the same molecular formula of atoms but the structure of the compounds are different for the positions of atoms are called isomers.

In double bond or cyclic compounds, if two same functional groups are present on the same side of the double bond or cyclic compound, the given compound can be labeled as cis.

If the two functional groups are present on the different sides of the double bond or cyclic compound, the given compound can be labeled as Trans.

Cis-trans isomerism exists in the compounds in which similar groups are present on the adjacent carbon atoms.

Chair conformations: It is the most stable conformation, which accurately shows the spatial arrangement of atoms.

Equatorial bonds are parallel to the average plane of the ring, while axial bonds are perpendicular to the average plane of the ring.

The conformation having bonds at the equatorial positions are more stable than those with bonds at the axial position.

On flipping the cyclohexane ring, axial bonds become equatorial bonds and equatorial bonds becomes axial bond.

Bulkier group acquires equatorial positions to form stable conformer due to steric factors.

A type of halogenation in which alkanes and aromatics, which are alkyl substituted, react chemically in presence of light is known as free radical halogenation. It involves chain initiation, propagation and termination steps in its whole mechanism.

Homolytic fission is that fission in which each atom in the bond has an electron which results in species called free radical.

In heterolytic fission, when covalent bond is broken, the shared pair of electron is taken by one of the atoms.

Blurred answer
Students have asked these similar questions
(1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amide
Write the reagent or draw structures of the starting material or organic product(s) in the following reactions. If more than one product is formed, identify the major product where possible. (a) (b) HO OH OH H2SO4 ? Cl₂ ? FeCl3
Compounds B and C are hydrocarbons with the structural formulae as shown below. CH, „CH, в (a) Name compounds B and C according to the IUPAC nomenclature. (b) Both B and C can undergo oxidation reaction with the same oxidizing agent. Write chemical equations involved and explain the differences between these two reactions. (c) Name one reaction that converts B to methylcyclohexane.
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning