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Methyl nitrite

Methyl nitrite burns vigorously with oxygen at atmospheric pressure giving a very fast flame. It will also support a very feeble, slow self-decomposition flame [122—124]. The latter is orange-red and the burning velocity [125], relative to the unburnt gas at 18 °C, is about 3.5 cm.sec , while the global activation energy [126] is 37.5 kcal.mole . The final products of the flame are represented by the stoichiometric equation [Pg.485]

CH3ONO = 0.72CO + O.56H2 + 0.54NO + O.42H2O + O.I4N2 + [Pg.485]

The flame temperature calculated on the basis of this stoichiometry is about 1100 °C, in excellent agreement with the observed value [127]. [Pg.485]


Example 24 Add. 1 mole of 3-(3,4-methylenedioxyphenyl) propylene,. 25 mole of methyl nitrite,. 008 mole palladium bromide as a catalyst,. 5L of methanol and 36g of water to a flask. Stir magnetically for 2 hoursat 25C. Yield of 3,4-methylenedioxyphenylacetone (also known as 3,4-... [Pg.82]

Example 86 A 0.10 mole amount of the starting 3-(4-hydroxyphenyl) propylene, 0.25 mole of methyl nitrite, 0.5 liter of methyl alcohol, and 0.006 mole of a palladium chloride catalyst were charged into a reaction vessel. Then, the reaction was carried out at a temperature of 20.degree. C. for 1.5hours."... [Pg.83]

A solution of chilled dilute H2SO4 (C) is dropped in a solution af methanol, water and NaN02 (B), then methyl nitrite is generated. [Pg.84]

The oxidation of terminal alkenes with an EWG in alcohols or ethylene glycol affords acetals of aldehydes chemoselectively. Acrylonitrile is converted into l,3-dioxolan-2-ylacetonitrile (69) in ethylene glycol and to 3,3-dimetho.xy-propionitrile (70) in methanol[28j. 3,3-Dimethoxypropionitrile (70) is produced commercially in MeOH from acrylonitrile by use of methyl nitrite (71) as a unique leoxidant of Pd(0). Methyl nitrite (71) is regenerated by the oxidation of NO with oxygen in MeOH. Methyl nitrite is a gas, which can be separated easily from water formed in the oxidation[3]. [Pg.31]

Methyl nitrite has the molecular formula CH3NO2 All hydrogens are bonded to carbon and the order of atomic connections is CONO... [Pg.20]

The structure shown is the best (most stable) Lewis structure for methyl nitrite All atoms except hydro gen have eight electrons (shared + unshared) in their valence shell... [Pg.20]

None of the atoms in the Lewis structure shown in step 6 possesses a formal charge An alternative Lewis structure for methyl nitrite... [Pg.20]

We can illustrate isomensm by referring to two different compounds mtromethane and methyl nitrite both of which have the molecular formula CH3NO2 Nitromethane... [Pg.23]

The two Lewis structures D and E of methyl nitrite satisfy the octet rule... [Pg.26]

Structure D has no separation of charge and is more stable than E which does The true structure of methyl nitrite is more like D than E... [Pg.26]

Nitromethane is stabilized by electron delocalization more than methyl nitrite is The two most stable resonance forms of nitromethane are equivalent to each other... [Pg.27]

The two most stable resonance forms of methyl nitrite are not equivalent... [Pg.27]

In addition to the Hquid-phase -butyl nitrite (BN) process, UBE Industries has estabHshed an industrial gas-phase process using methyl nitrite (50—52). The oudine of the process is described in Eigure 4 (52). This gas-phase process is operated under lower reaction pressure (at atmospheric pressure up to 490 kPa = 71 psi) and is more economical than the Hquid-phase process because of the foUowing reasons owing to the low pressure operation, the consumption of electricity is largely reduced (—60%) dimethyl oxalate (DMO) formation and the methyl nitrite (MN) regeneration reaction are mn... [Pg.459]

Methyl nitrite [624-91-9] M 61.0, b -12 , d (liq) 0.991. Condensed in a liquid nitrogen trap. Distd under vacuum, first trap containing dry Na2C03 to free it from acid impurities then into further Na2C03 traps before collection. [Pg.296]

CH3N02 methyl-nitrite -65.640 2.2023E-01 9.2945E-06 1.00 73 C2H5CL CHLOROETHANE -112.949 1.7104E-01 1.9992E-05 -60.00... [Pg.377]

Methyidichloroarsine Methylene glycol dinitrate Methyl ethyl ketone peroxide, >50% alpha-Methylglucoside tetranitrate alpha-Methylglycerol trinitrate Methyl nitramine (dry) metal salts of Methyl nitrate Methyl nitrite... [Pg.475]

We can illustrate isoimeiisim by refening to two different coimpounds, nitromethane and methyl nitrite, both of which have the molecula fonmula CH3NO2. Nitromethane,... [Pg.23]


See other pages where Methyl nitrite is mentioned: [Pg.202]    [Pg.20]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.26]    [Pg.481]    [Pg.566]    [Pg.602]    [Pg.626]    [Pg.459]    [Pg.248]    [Pg.74]    [Pg.157]    [Pg.232]    [Pg.1026]    [Pg.20]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.26]   
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Alkyl nitrites methyl nitrite

Apparatus for nitrosation with methyl nitrite

Methyl isocyanate nitrite

Methyl nitrite, atmosphere

Methyl nitrite, from methanol reaction

Methyl nitrite, photolysis

Methyl radical nitrite esters

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