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Slide 1
Slide 1

... the acid and alcohol in the presence of a small quantity of acid catalyst (H2SO4 or HCl (g)) causes ester formation (esterification) along with dehydration. The equilibrium constant is not large (Keq ~ 1) but high yields can be obtained by adding a large excess of one of the reactants and removing t ...
1 Chapter 21: Organic and Biochemical Molecules
1 Chapter 21: Organic and Biochemical Molecules

Chemistry 162 Workbook 10.6
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... experience   with   testing   environments.   Once   the   student   has   completed   an   exam,   the   tutor   may   choose   to   grade   the   exam   during   a   normal   session   while   the   student   works   on   other   materials ...
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Atmospheric Formation_TELTEK

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Pdf - Text of NPTEL IIT Video Lectures
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... The d electron from the ruthenium atom is excited to the byp anti-bonding orbital. So, we have this bipyridine ligand. So, this is the by tented n n donor ligand what we have in our hand and this is attached to one ruthenium, so 3 such ruthenium species is there and these are all neutral. So, from t ...
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Organic for Forensic Science

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Noble, Abigail E., Carl H. Lamborg, Dan C. Ohnemus, Phoebe J

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... The addition of a nucleophile to a polar CO bond is the key step in three of the four major carbonyl-group reactions. We saw in Chapter 19 that when a nucleophile adds to an aldehyde or ketone, the initially formed tetrahedral intermediate either can be protonated to yield an alcohol or can elimina ...
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... and 12% yield, respectively. This procedure relies on the performance of double and threefold Ugi4CR-based macrocyclizations that furnish the dimeric and trimeric N-substituted cyclocholamides 18 and 19, respectively. The corresponding tetramer was formed only in traces as detected by ESI-MS, but it ...
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... • Methyl halides: only one C, CH3X • Primary: C to which X is bonded has only one C-C bond. • Secondary: C to which X is bonded has two C-C bonds. • Tertiary: C to which X is bonded has three C-C bonds. ...
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Document

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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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