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to get Period 2 8
to get Period 2 8

Organic Reactions
Organic Reactions

... • Esterification is the most common type of condensation reaction on the regents exam. • Protein synthesis is a commonly cited example of condensation. ...
Carbon Chemistry
Carbon Chemistry

Ch 19 test_take-home
Ch 19 test_take-home

Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry
Chem 30BL_Lecture 2_.. - UCLA Chemistry and Biochemistry

C1_Revision_Sheets[1] - Chew Valley School | Intranet Homepage
C1_Revision_Sheets[1] - Chew Valley School | Intranet Homepage

... Less reactive metals are displaced by carbon. Complete the equation below and then make your own one: Copper Oxide + Carbon ...
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry
Chem 30BL * Lecture 2 - UCLA Chemistry and Biochemistry

Carbon Compounds
Carbon Compounds

PART 3 Principles and Applications of Organometallics in Catalysis
PART 3 Principles and Applications of Organometallics in Catalysis

Study Guide on Ch 5 and 6
Study Guide on Ch 5 and 6

... B. Fischer Projection vs Wedge-and-dash (p. 219) ...
Organic and Biological Molecules
Organic and Biological Molecules

Organometallic Compounds and Catalysis: Synthesis
Organometallic Compounds and Catalysis: Synthesis

Unit 2 Content Statements
Unit 2 Content Statements

MS PowerPoint - Catalysis Eprints database
MS PowerPoint - Catalysis Eprints database

COUPLING REACTIONS IN ORGANIC SYNTHESIS
COUPLING REACTIONS IN ORGANIC SYNTHESIS

... Figure OA1.5. A reductive elimination of a methyl and a hydride to form methane. The addition of dihydrogen to Vaska's complex and other transition metals is a reversible reaction. The hydrogen can be released again if the reaction moves to the left in a reductive elimination. That reversibility mak ...
Methane - ARZELORIVAS IS
Methane - ARZELORIVAS IS

I. Hydrocarbons I. Hydrocarbons I. Hydrocarbons I
I. Hydrocarbons I. Hydrocarbons I. Hydrocarbons I

Saturated Hydrocarbon
Saturated Hydrocarbon

Chem 2641 Chapter 5 Understanding Organic Reactions I. Writing
Chem 2641 Chapter 5 Understanding Organic Reactions I. Writing

Unit 8 – Organic Chemistry
Unit 8 – Organic Chemistry

Materials Seminar Professor Carsten Sievers Georgia Institute of  Technology
Materials Seminar Professor Carsten Sievers Georgia Institute of Technology

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Reactions of Hydrocarbons & their functional groups
Reactions of Hydrocarbons & their functional groups

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Pre Ch15 HW

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Redox Reactions

< 1 ... 42 43 44 45 46 47 48 49 50 ... 53 >

Cracking (chemistry)



In petroleum geology and chemistry, cracking is the process whereby complex organic molecules such as kerogens or heavy hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carbon-carbon bonds in the precursors. The rate of cracking and the end products are strongly dependent on the temperature and presence of catalysts. Cracking is the breakdown of a large alkane into smaller, more useful alkanes and alkenes. Simply put, hydrocarbon cracking is the process of breaking a long-chain of hydrocarbons into short ones. More loosely, outside the field of petroleum chemistry, the term ""cracking"" is used to describe any type of splitting of molecules under the influence of heat, catalysts and solvents, such as in processes of destructive distillation or pyrolysis. Fluid catalytic cracking produces a high yield of petrol and LPG, while hydrocracking is a major source of jet fuel, Diesel fuel, naphtha, and again yields LPG.
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