Propyl iodides

Consider the reaction of ethyl propyl ether with HI. Write the two different possible product combinations. Compare e energies of the two products 1-propanol and ethyl iodide-, ethanol and 1-propyl iodide). Which is the lower-energy combination Is the energy difference significant (>.002 au or 1 kcal/mol) Based on thermochemistry alone, is this reaction Likely to be selective Explain. 

Vibrational spectra assigned to surface 1-propyl groups following the decomposition of 1-propyl iodide or bromide have been obtained as follows, where the surface used, the halide precursor, and the decomposition temperatures are all indicated Al(100), iodide, 310 K (199) Cu(lll), bromide, 180 K (200) Cu(lll), iodide, 180 K (201) Cu(100), bromide, 185 K (193) and Cu(110), iodide, 165 K (202). The first four cases were investigated by VEELS, and the fifth one by RAIRS. The band positions observed, the band intensities, and their probable vibrational assignments are listed in... 

Lithioethenyl phenyl tellurium was not alkylated by 1-propyl iodide or allyl bromide. Only diphenyl ditellurium and ethenyl phenyl tellurium were isolated from the reaction mixtures1. 

Deghenghi et al studied the reductive alkylation of 16-dehydropregneno-lone acetate in ammonia-tetrahydrofuran using excess lithium and alkyl iodides. Alkylation with methyl iodide followed by reacetylation of the 3-hydroxyl group affords 17a-methylpregnenolone acetate in 20% yield after purification by column chromatography. Ethyl iodide affords the 17a-ethyl analog in 40% yield, but n-propyl iodide affords the 17a-propyl compound in only a 12 % yield. 

C10H21N 6192-97-8) see Barbexaclone propyl homovanillate sodium salt (C 2Hi5NaO ) see Propanidid D-6-propyl-8(i-hydroxymethylergoline (C11H24N2O 63719-21-1) see Pergolide propyl iodide... 

Jso-propyl lactate has been prepared by heating iso-propyl alcohol and lactic acid in a sealed tube at 1700,1 2 and from silver lactate and iso-propyl iodide, together with the iso-propyl ester of a-iso-propoxy-propionic acid.3 Direct esterification of the acid with the alcohol, with sulfuric acid, has failed to give a yield greater than 20 per cent of the theoretical amount, and the product has been less pure. 

Phosphorus tribromide Phosphorus trichloride Propionic acid Propyl acetate Propyl alcohol Propyl bromide Propyl chloride Propyl formate Propyl iodide Sodium... 

The propyl chlorides, propyl bromides, and propyl iodides are all liquids. 

Propyl iodide, i48 Propyl mercaptan, pi 98 6-Propyl-2-thiouracil, hi 40 Pseudocumene, t358 Pyrene, b52... 

The gas-phase reactions of the fulvene radical cation with neutral 1,3-butadiene, alkenes and 2-propyl iodide have been investigated by Russell and Gross131a using ICR mass spectrometry. Unlike ionized benzene, ionized fulvene undergoes no C—C coupling with 2-propyl iodide. On the basis of deuterium and 13C labelling, the reaction of ionized fulvene with 1,3-butadiene was suggested to occur by [6 + 4] cycloaddition to yield tetrahydroazulene radical cations. Cycloadditions of neutral fulvene were also studied in this work. 

FLUOROPROPANE ISOPROPYL IODIDE n-PROPYL IODIDE ALLYAMINE PROPYLENEIMINE N,N-DIMETHYLFORMAMIDE M-METHYLACETAMIDE... 

Synonyms AI3-28594 BRN 0505937 CCRIS 542 EINECS 203-460-2 Propyl iodide /j-Propyl... 

Propylbenzene, see Propylbenzene Propyl carbinol, see 1-Butanol Propylene aldehyde, see Acrolein, Crotonaldehyde Propylene chloride, see 1,2-Dichloropropane Propylene dichloride, see 1,2-Dichloropropane a,p-Propylene dichloride, see 1.2-Dichloropropane 1,2-Propylene oxide, see Propylene oxide Propyl ester of acetic acid, see Propyl acetate Propylethylene, see 1-Pentene 5-Propylhexane, see 4-Methyloctane Propyl hydride, see Propane Propylic alcohol, see 1-Propanol Propyl iodide, see 1-Iodopropane n-Propyl iodide, see 1-Iodopropane Propylmethanol, see 1-Butanol Propyl methyl ketone, see 2-Pentanone n-Propyl nitrate, see Propyl nitrate... 

Olivetol. (5-Alkyl Resourcinol) BER 69, 1644 (1936). Mix 25 g of ethyl-3,4,5-trimethoxy benzoyl acetate and 2.0 g of clean sodium in 100 ml ethanol and warm to react. Add 2 g n-propyl iodide (this may be replaced with n-amyl iodide) and heat on a steam bath for 12 hours, then neutralize and remove the ethanol by distillation. Extract the residue with ether, dry, and evaporate in vacuo to get 30 g of the alkyl acetate. Heat 22 g of this acetate in 5% KOH ethanolic solution for 1 hour at 50° and let stand to precipitate 14 g of 3,4,5-trimethoxyvalerophenone. Mix 11 g of the above product with 60 g of sodium in 600 ml ethanol. Warm and after dissolving the sodium add 2 liters of water. M e acidic with HCl acid and remove the ethanol by distillation. Extract with ether, dry, and evaporate the ether in vacuo to get if. g olivetol dimethyl ether. To demethylate this ether add it to 70 ml of hydrogen iodide and heat to boiling and reflux for two hours. Distill and keep the fraction at 160°-170° with 3-4 mm of vacuum applied to the distillation set-up. Yield about 6 g. 

Unfortunately, we lack measured enthalpy of formation values for most organic iodides of interest here except for ethyl, n-propyl and phenyl iodides. From equation 14 and with phenyl iodide in its reference liquid state and with ethyl and propyl iodides in their reference gaseous states, the enthalpies of formation of ethyl lithium and of n-propyl lithium are calculated to be ca —54 and —74 klmoP, respectively. The former value is the same as those from Table 1 and the latter is compatible with one of the other values for n-propyl lithium derived in earlier sections. 

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