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... • Fuels (e.g. the RM1.92 RM2.10 Ron95) are made up mostly of alkanes. In excess oxygen • CnH2n+2 + (1.5n+½)O2  nCO2 + (n+1)H2O ...
Homework Booklet Unit 1 Feb14
Homework Booklet Unit 1 Feb14

... (c) Name the two pollutant gases changed by the catalyst and describe what they are changed into. 4. Explain why solid citric acid does not conduct electricity yet when it dissolves in water it does conduct. 5. Electrolysis of acids can be used to confirm the presence of hydrogen ions. (a) At which ...
Part I - American Chemical Society
Part I - American Chemical Society

... May 1, 2007, after which tests can be returned to students and their teachers for further study. Allow time for the student to read the directions, ask questions, and fill in the requested information on the Scantron sheet. The answer sheet must be completed using a pencil, not pen. When the student ...
Descriptive Chemistry for Midterm Exam #1
Descriptive Chemistry for Midterm Exam #1

Synthesis and characterization of a nano Cu2 cluster
Synthesis and characterization of a nano Cu2 cluster

... was to incorporate Pb into the present system and make a new high nuclearity heteronuclear Cu-Pb cluster with magnetic or antibacterial properties. For its synthesis, first Cu (NO3)2.3H2O (2mmol) and PhCOOH (10mmol) was dissolved in a mixed solvent MeCN/EtOH (10/10, v/v); separately Pb(NO3)2 (1mmol) ...
Ch. 4 Carbon
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...  They behave consistently and characteristically, giving unique properties to the molecules possessing them. ...
Science 30 Chemistry
Science 30 Chemistry

... Alcohols and carboxylic acids react to form esters An H is removed from the alcohol and an ‘OH’ from the acid- water is formed. Functional group for ester: Naming an ester:  R’ is the alcohol, change the ending to ‘yl’  R is the acid – drop ‘ic acid’ and change ending to ‘ate’ ...
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Ch04-04-alkenes-2

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IB Chemistry Review. Unit I. Topics 2

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Topic 1 Review - Capital High School

... (ii) Compare the relative polarities of the C–H bond in ethene and the N–H bond in hydrazine. (iii) Hydrazine is a polar molecule and ethene is non-polar. Explain why ethene is nonpolar. (c) The boiling point of hydrazine is much higher than that of ethene. Explain this difference in terms of the in ...
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Summary of AS-level Paper 2 content - A

... I can distinguish between thermal cracking (takes place at high pressure and high temperature and produces a high percentage of alkenes) and catalytic cracking (takes place at a slight pressure, high temperature and in the presence of a zeolite catalyst and is used mainly to produce motor fuels and ...
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Every reaction is reversible: A chemical reaction is in equilibrium

... Nitrogen or Helium. The carrier gas drags the mixture into a heated coil packed with the stationery phase - a liquid (e.g. a silicone oil) held on a solid support (e.g. Celite). Careful control of the oven temperature ensures that volatile liquids in the mixture quickly become gaseous. The gas mixtu ...
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Chapter 12 Alcohols, Phenols, Ethers, Aldehydes, and Ketones

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IOSR Journal of Applied Chemistry (IOSR-JAC)

... to enable the mammary glands to secrete lactose. However, most lactose in breast milk is synthesized from galactose taken up from the blood and only 35 ± 6% is made from galactose from De-novo synthesis [1]. In human body the main pathway of D(+)- Galactose metabolism is the Leloir pathway [2]. Howe ...
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... 7. Tri-Iodomethane (Iodoform) Formation *Note: Reaction is only positive for alcohol containing a methyl group and a hydrogen atom attached to the carbon at which the hydroxyl group is also attached. ...
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... this fast pre-equilibrium). The model does not imply a different operative mechanism to the well-known coordination– insertion process, but rather reflects a different rate-determining step. In the present case, monomer saturation kinetics are rationalized by the steric hindrance of the HMDS ligand ...
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C7 Revision Powerpoint Part 1

... 2. Describe how the functional group affects the property of an organic compound and understand that alkanes are unreactive towards aqueous reagents because C—C and C—H bonds are unreactive; 3. Write balanced chemical reactions including for ...
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... substituents ortho and para react with nucleophiles • Form addition intermediate (Meisenheimer complex) that is stabilized by electron-withdrawal • Halide ion is lost to give aromatic ring ...
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Unit-8-Alcohols-Aldehydes-Ketones

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Kinetics of Oxidation of Aliphatic Alcohols by Potassium Dichromate

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Synthesis of first row transition metal carboxylate complexes by ring

... which the dicarboxylates are at para position to each other. The cationic part is a complex cation of tetra-aqua (2,2 -bipyridine)nickel(II). Thus, the inorganic complexes obtained from these ring opening reactions are decided by the ancillary ligands. However, in both the cases we had other unchar ...
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Introducton of Organic Chemistry in Healthy Sciences ( by Dr. Alaa J

... Question : Why, then, do we pay such special attention to just one element from among 116? The first reason is largely historical. In the early days of chemistry, scientists thought organic compounds were those produced by living organisms, and that inorganic compounds were those found in rocks and ...
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Chemical Reactions: Helpful Hints

... Reaction 15a is a special type of redox reaction - a combustion reaction. The terms "oxidant" or "oxidation" are derived from oxygen (O2), the gas that allows us to live in our atmosphere. In this reaction, you're reacting magnesium metal with oxygen at a high temperature - this reaction is describe ...
Organic Compounds
Organic Compounds

... Solubility in inorganic solvent (water) Solubility in organic ...
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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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