Principles of Instrumental Analysis, 6th Edition
Principles of Instrumental Analysis, 6th Edition
6th Edition
ISBN: 9788131525579
Author: Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher: Cenage Learning
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Chapter 18, Problem 18.6QAP
Interpretation Introduction

(a)

Interpretation:

The circumstances under which a helium-neon laser would be preferable to an argon-ion laser should be determined.

Concept introduction:

The helium-neon laser is working at a wavelength of 632.8nm. It contains 25% of neon and 75% of helium. The Argon-ion laser is a powerful gas laser. It generates multiples colour beam such as green or blue beam.

Interpretation Introduction

(b)

Interpretation:

The circumstances under which a diode laser would be preferable to an argon-ion laser or helium-neon laser should be determined.

Concept introduction:

The diode laser is a light creating device. It is uses semiconductor technology. It can convert electrical energy directly to the light. The helium-neon laser is working at a wavelength of 632.8nm. It contains 25% of neon and 75% of helium. The Argon-ion laser is a powerful gas laser. It generates multiples colour beam such as green or blue beam.

Interpretation Introduction

(c)

Interpretation:

The reasons of UV emitting sources are avoided should be determined.

Concept introduction:

UV rays are visible radiation as such as visible light, signals. Ultraviolet (UV) rays are electromagnetic radiation which transmitted with different frequencies.

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Give the product of the bimolecular elimination from each of the isomeric halogenated compounds. Reaction A Reaction B. КОВ CH₂ HotBu +B+ ко HOIBU +Br+ Templates More QQQ Select Cv Templates More Cras QQQ One of these compounds undergoes elimination 50x faster than the other. Which one and why? Reaction A because the conformation needed for elimination places the phenyl groups and to each other Reaction A because the conformation needed for elimination places the phenyl groups gauche to each other. ◇ Reaction B because the conformation needed for elimination places the phenyl groups gach to each other. Reaction B because the conformation needed for elimination places the phenyl groups anti to each other.
Five isomeric alkenes. A through each undergo catalytic hydrogenation to give 2-methylpentane The IR spectra of these five alkenes have the key absorptions (in cm Compound Compound A –912. (§), 994 (5), 1643 (%), 3077 (1) Compound B 833 (3), 1667 (W), 3050 (weak shoulder on C-Habsorption) Compound C Compound D) –714 (5), 1665 (w), 3010 (m) 885 (3), 1650 (m), 3086 (m) 967 (5), no aharption 1600 to 1700, 3040 (m) Compound K Match each compound to the data presented. Compound A Compound B Compound C Compound D Compound
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