Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 2, Problem 2.28AP
Interpretation Introduction

(a)

Interpretation:

The structure of an alkane or cycloalkane that has more than three carbons and only primary hydrogens is to be drawn.

Concept introduction:

The carbons in a chemical formula may or may not be branched. The branched carbons are categorized as primary, secondary, tertiary, and quaternary carbons depending on the substituent attached to it. The branched carbons are categorized to understand the chemical reactions in which these carbons are involved.

Interpretation Introduction

(b)

Interpretation:

The structure of an alkane or cycloalkane has five carbons and only secondary hydrogens is to be drawn.

Concept introduction:

The carbons in a chemical formula may or may not be branched. The branched carbons are categorized as primary, secondary, tertiary, and quaternary carbons depending on the substituent attached to it. The branched carbons are categorized to understand the chemical reactions in which these carbons are involved.

The hydrogens attached to branched carbons are also categorized as primary, secondary and tertiary hydrogens.

Interpretation Introduction

(c)

Interpretation:

The structure of an alkane or cycloalkane has only tertiary hydrogens is to be drawn.

Concept introduction:

The carbons in a chemical formula may or may not be branched. The branched carbons are categorized as primary, secondary, tertiary, and quaternary carbons depending on the substituent attached to it. The branched carbons are categorized to understand the chemical reactions in which these carbons are involved.

The hydrogens attached to branched carbons are also categorized as primary, secondary and tertiary hydrogens.

Interpretation Introduction

(d)

Interpretation:

The structure of an alkane or cycloalkane that has a molecular mass of 84.2 is to be drawn.

Concept introduction:

The carbons in a chemical formula may or may not be branched. The branched carbons are categorized as primary, secondary, tertiary, and quaternary carbons depending on the substituent attached to it. The branched carbons are categorized to understand the chemical reactions in which these carbons are involved.

The hydrogens attached to branched carbons are also categorized as primary, secondary and tertiary hydrogens.

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Q1: Curved Arrows, Bronsted Acids & Bases, Lewis Acids & Bases Considering the following reactions: a) Predict the products to complete the reactions. b) Use curved electron-pushing arrows to show the mechanism for the reaction in the forward direction. Redraw some of the compounds to explicitly illustrate all bonds that are broken and all bonds that are formed. c) Label Bronsted acids and bases in the left side of the reactions. Label conjugate acids and bases in the right side of the reactions. d) Label Lewis acids and bases, nucleophiles and electrophiles in the left side of the reactions. A. + OH CH30: OH B. + HBr C. H₂SO4 D. CF 3. CH 3 + HCI N H fluoxetine antidepressant 1↓ JDownload
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Part 3: AHm,system Mass of 1.00 M HCI Vol. of 1.00 M HCI Mass of NaOH(s) Total Mass in Calorimeter Mole product if HCI limiting reactant Trial 1 62.4009 1.511g Mole product if NaOH limiting reactant Limiting reactant Initial Temperature Final Temperature 23.8°C 37.6°C Change in Temperature AHm,system (calculated) Average AHm,system (calculated) (calculated) (calculated) Trial 2 64.006g 1.9599 (calculated) (calculated) (calculated) (calculated) (calculated) (calculated) 24.7°C 41.9°C (calculated) (calculated) (2 pts. each)
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