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Structure and Bonding
Structure and Bonding

... hydrogen over a finely alkanes divided metal catalyst such as palladium, nickel, or platinum. This is an addition reaction since it involves the addition of hydrogen atoms to each end of the double bond. It is also called a catalytic hydrogenation or a reduction reaction. The catalyst is crucial sin ...
CHEM_2nd_Semester_Final_R eview
CHEM_2nd_Semester_Final_R eview

... 40. What happens to atoms or molecules as their temperature is increased? 41. Describe heat flow. 42. What is the difference between an exothermic reaction and an endothermic reaction? 43. Draw an energy diagram for an endothermic and exothermic reaction. 44. Are the following changes of state exoth ...
Chemistry 2nd Semester Final Exam Review Chemical Bonds Give
Chemistry 2nd Semester Final Exam Review Chemical Bonds Give

... 40. What happens to atoms or molecules as their temperature is increased? 41. Describe heat flow. 42. What is the difference between an exothermic reaction and an endothermic reaction? 43. Draw an energy diagram for an endothermic and exothermic reaction. 44. Are the following changes of state exoth ...
2nd Semester Final Review
2nd Semester Final Review

... 40. What happens to atoms or molecules as their temperature is increased? 41. Describe heat flow. 42. What is the difference between an exothermic reaction and an endothermic reaction? 43. Draw an energy diagram for an endothermic and exothermic reaction. 44. Are the following changes of state exoth ...
Preparation of Aldehydes and Ketones
Preparation of Aldehydes and Ketones

... Water hydrates the carbonyl group. The addition of water to an aldehyde or ketone is catalyzed by either acid or base. The equilibrium reaction forms geminal diols, also called carbonyl hydrates: ...
ANAEROBIC PROCESSES
ANAEROBIC PROCESSES

esters - wellswaysciences
esters - wellswaysciences

... © Pearson Education Ltd 2009 This document may have been altered from the original ...
ALKENES Introduction • Unsaturated hydrocarbons containing C=C
ALKENES Introduction • Unsaturated hydrocarbons containing C=C

Practice Questions for Chapters 1-8 CHEM 4000A
Practice Questions for Chapters 1-8 CHEM 4000A

Catalysis Web Pages for Pre-University
Catalysis Web Pages for Pre-University

... correct temperature (~400-450 oC ) and high pressure. The catalyst is simply iron. 3H2 + N2 ⇌ 2NH3 The catalyst does not increase the yield of the reaction but just decreases the time it takes to reach equilibrium. At equilibrium the catalyst increases the rate of the reaction reactants to products ...
Lecture12
Lecture12

... optimal conditions for every new substrate Reactions are easily poisoned by molecular oxygen ...
Samantha Landolfa Amy Ryan Section 10 Experiment 9 – Alkenes
Samantha Landolfa Amy Ryan Section 10 Experiment 9 – Alkenes

... In this experiment, 2-methyl-2-butanol is dehydrated to produce a mixture of two isomers that can be analyzed by gas chromatography. The dehydration of the alcohol is accomplished via an E1 elimination reaction. The rates of reactivity are tertiary > secondary > primary. An E1 reaction is favored wh ...
Acid a substance that produces hydrogen ions in aqueous solution
Acid a substance that produces hydrogen ions in aqueous solution

Organic Chemistry
Organic Chemistry

... Nomenclature for Alkenes 1. Root hydrocarbon name ends in -ene C2H4 is ethene 2. With more than 3 carbons, double bond is indicated by the lowest numbered carbon atom in the bond. C=CCC is 1-butene ...
CHEM 122: Introduction to Organic Chemistry Chapter 9: Aldehydes
CHEM 122: Introduction to Organic Chemistry Chapter 9: Aldehydes

... a) Cyclohexanone and aniline b) Cyclohexene and cyclohexanol c) Benzaldehyde and cinnamaldehyde 23. 5-Hydroxyhexanal forms a six-membered cyclic hemiacetal, which predominates at equilibrium in aqueous solution. a) Draw a structural formula for this cyclic hemiacetal. b) How many stereoisomers are p ...
Ch 12 Alcohols and Thiols
Ch 12 Alcohols and Thiols

... 2. Van der Waals – depending on Carbon chain length • Length of Carbon chain • C1-C2 gas, C3 -C10: liquid, C11 and higher: solids ...
Organic Nomenclature - Alkanes, Alkenes, Alkynes
Organic Nomenclature - Alkanes, Alkenes, Alkynes

... Naming Ketones (–C=O group) = -one ending Ketones are very similar to aldehydes. The only difference is that the C=O in a ketone is in the middle of a chain - not on the terminal carbon. To name a ketone, use the -one ending and specify the position of the C=O with a number at the beginning of the n ...
hydrocarbons summary
hydrocarbons summary

... There are common names for many organic compounds. For example: methyl alcohol, acetylene, acetic acid, etc. Yet, there are an infinite number of possible organic structures. Thus, it is important to name them in a systematic way. The purpose of IUPAC names is to provide a set of rules so that the s ...
SCH4U Unit Test Name
SCH4U Unit Test Name

... a. the smallest aldehyde has the formula HCOH b. a carbonyl carbon consists of a carbon-oxygen double bond c. in an aldehyde, the carbonyl carbon is always bonded to a hydrogen atom d. Ketones are more soluble in water than alcohols with the equivalent number of carbons ____ 17. The correct name for ...
File
File

... _____ 14. The activity series of metals can be used to predict products in double-replacement reactions. _____ 15. Carbon dioxide and water are the products of the combustion of hexane (C6H14). _____ 16. A nonmetal can replace another nonmetal from a compound in a single-replacement reaction. ...
A NEW APROACH TO N-SUBSTITUTED OXAZOLIDINE VIA NITRILIUM ION TRAPPING
A NEW APROACH TO N-SUBSTITUTED OXAZOLIDINE VIA NITRILIUM ION TRAPPING

... Abstract: We have recently demonstrated a direct conversion of secondary alcohols to amides with retention of configuration. This method involved the in situ formation of chlorosulfites followed by a reaction with nitrile complexes of Ti(IV) fluoride. We hypothesize that these amidation reactions in ...
Document
Document

Organic Reactions
Organic Reactions

Organometallic Chemistry
Organometallic Chemistry

... In other cases, a reduction of a metal precursor in the presence of CO (or using CO as the reductant) is used (Equations 2-3). Carbon monoxide also reacts with various metal complexes, most typically filling a vacant coordination site (Equation 4) or performing a ligand substitution ...
Exam 1
Exam 1

... (i) Starting with t-butyl alcohol, show the reaction mechanism to produce an ether in acidic conditions. What is the name of this ether? (ii) Starting with sodium t-butoxide and bromoethane, show the reaction mechanism required to produce an ether in basic reaction conditions. What is the name of th ...
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Hydroformylation



Hydroformylation, also known as oxo synthesis or oxo process, is an important homogeneously catalyzed industrial process for the production of aldehydes from alkenes. This chemical reaction entails the addition of a formyl group (CHO) and a hydrogen atom to a carbon-carbon double bond. This process has undergone continuous growth since its invention in 1938: Production capacity reached 6.6×106 tons in 1995. It is important because the resulting aldehydes are easily converted into many secondary products. For example, the resulting aldehydes are hydrogenated to alcohols that are converted to plasticizers or detergents. Hydroformylation is also used in specialty chemicals, relevant to the organic synthesis of fragrances and natural products. The development of hydroformylation, which originated within the German coal-based industry, is considered one of the premier achievements of 20th-century industrial chemistry.The process typically entails treatment of an alkene with high pressures (between 10 to 100 atmospheres) of carbon monoxide and hydrogen at temperatures between 40 and 200 °C. Transition metal catalysts are required.
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