Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
Question
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Chapter 15, Problem 15.36SP

(a)

Interpretation Introduction

Interpretation:

The pi molecular orbitals of hexa-1,3,5-triene is to be drawn.

Concept introduction:

Molecular orbital diagrams are used for determining the bonding in molecules using linear combination of atomic orbitals. The number of molecular orbitals formed is equal to the number of atomic orbitals that combine with each other.

(b)

Interpretation Introduction

Interpretation:

The electronic configuration of the ground state of hexa-1,3,5-triene is to be stated.

Concept introduction:

Molecular orbital diagrams are used for determining the bonding in molecules using linear combination of atomic orbitals. The number of molecular orbitals formed is equal to the number of atomic orbitals that combine with each other.

(c)

Interpretation Introduction

Interpretation:

The product that would result from the [6+2] cycloaddition of hexa-1,3,5-triene with maleic anhydride is to be stated.

Concept introduction:

A chemical reaction in which cyclic product is formed from conjugate system is known as cycloaddition reaction.

(d)

Interpretation Introduction

Interpretation:

The [6+2] cycloaddition of hexa-1,3,5-triene with maleic anhydride is thermally forbidden but photochemically allowed is to be stated.

Concept introduction:

Molecular orbital diagrams are used for determining the bonding in molecules using linear combination of atomic orbitals. The number of molecular orbitals formed is equal to the number of atomic orbitals that combine with each other.

(e)

Interpretation Introduction

Interpretation:

The Diels-Alder product that would result from heating hexa-1,3,5-triene with maleic anhydride is to be stated.

Concept introduction:

A chemical reaction that involves [4+2] cycloaddition is called Diels-Alder reaction. The reactant molecules that give rise to product are diene and dienophile.

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Choose the structure that fits the descriptions below from the pool of choices. 1. An isolated diene 2. an alkene with possible rearrangement product (1,2-H shift) with reaction to HI 3. a diene capable of having 1,2 and 1,4-addition products 4.
3. Choose the answer that satisfy each statement. a. Under thermal conditions, (2E,4Z)-hexadiene undergoes a ring closure to form b. Under photochemical conditions, (2E,4Z)-hexadiene undergoes a ring closure to form A) conrotatory, cis-3,4-dimethylcyclobutene B) conrotatory, trans-3,4-dimethylcyclobutene C) disrotatory, cis-3,4-dimethylcyclobutene D) disrotatory, trans-3,4-dimethylcyclobutene
1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE". H CI H3C SH T. H CI, ОН H3CH2C НО D D EN C(CH3)3 CH3 Me H Et N' 'N' C=C H3C Et Me what Columbus sought in the 'Indies' - Piperine CH2OH Br (H3C);C, H3C HOH, CH,CF, H3C Br HOH2C НО H the spice Columbus found (Capsaicin) HO. Muscalure Bombykol (the sex attaractant for the male silkworm) (the sex attaractant for the common housefly) OH .CO2H the "heart healthy" part of olive oil a 'less healthy' trans fatty acid from trans fat

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Organic Chemistry (9th Edition)

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