Quantitative Chemical Analysis
Quantitative Chemical Analysis
9th Edition
ISBN: 9781464135385
Author: Daniel C. Harris
Publisher: W. H. Freeman
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Chapter 3.4, Problem 5TY
Interpretation Introduction

Interpretation:

When the uncertainty in given pH is doubled, the relative uncertainty in [H+] has to be calculated.

Concept Introduction:

Exponents and logarithm:

Consider, y=antilog xy=10x .

Here, the relative uncertainty in y is proportional to the absolute uncertainty in x.

Uncertainty for 10x:        y =10xeyy =(ln 10)ex 2.3026ex

To Calculate: The relative uncertainty in [H+] when the uncertainty in given pH is doubled.

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Draw the structure of ,-diethyl--propylthiopentane.  With explanation
A. Provide a stepwise mechanism for the formation of nerolidyl pyrophosphate fromfarnesylpyrophosphate B. Provide a stepwise mechanism for the formation of carbocation 1 from nerolidylpyrophosphate. Number the backbone carbons of nerolidyl pyrophosphate from 1 to 11 as shown, andinclude the carbon numbering in your structure of 1 C. Following from B, give an arrow-pushing mechanism to convert 1 to 2 and 2 to 3. Use thebackbone carbon numbering from 1 to indicate where carbon atoms ended up in 2 and 3 D. In addition to forming epi-cedrol, carbocation 3 gives three minor byproducts: a diastereomericalcohol and two alkenes. Draw mechanisms that could give rise to these three products
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