Chemistry Talk Chemistry Talk    FAQ   Search   Memberlist   Usergroups   Register   Profile   Log in to check your private messages   Log in  Organic NO2 analogs Goto page 1, 2  Next          Chemistry Talk Forum Index -> Chemistry Talk View previous topic :: View next topic   Author Message hanson Guest Posted: Fri May 25, 2007 7:25 pm    Post subject: Organic NO2 analogs There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? Quote: Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson Back to top   Ads Advertising Sponsor Uncle Al Guest Posted: Fri May 25, 2007 7:58 pm    Post subject: Re: Organic NO2 analogs hanson wrote: Quote: There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson Idiot. A real man goes for RSF5 and aluminum or magnesium. -- Uncle Al http://www.mazepath.com/uncleal/ (Toxic URL! Unsafe for children and most mammals) http://www.mazepath.com/uncleal/lajos.htm#a2 Back to top   Ads Advertising Sponsor hanson Guest Posted: Fri May 25, 2007 9:37 pm    Post subject: Re: Organic NO2 analogs Idiot "Uncle Al" <UncleAl0@hate.spam.net> wrote in message news:4656F9AF.4846BA46@hate.spam.net... Quote: hanson wrote: http://groups.google.com/group/sci.physics/msg/59893aec79181fa8 There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. Quote: Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF Quote: Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? Quote: Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson Quote: [Idiot Al] Idiot. A real man goes for RSF5 and aluminum or magnesium. [hanson] ahahaha... your beytsim must have fallen off and gummed up your work if THAT is the answer from uncle Al, the severely gifted idiot. Your ejaculate does not even address the question because you have that certain uncertainty about your own masculinity which seems to loom large on your idiot and Benzilated mind... ahahaha... There must be too much aluminum in your brain, Al..... tzheimer. My questions pertains to... well, you wouldn't understand, idiot Thanks for the laughs, Schwartz... ahahaha.... Quote: Now does anybody know?.. There must be more than just idiots like Schwartz on the Usenet. Back to top   Ads Advertising Sponsor Androcles Guest Posted: Fri May 25, 2007 9:58 pm    Post subject: Re: Organic NO2 analogs "hanson" <hanson@quick.net> wrote in message news:UgE5i.1781$XC3.386@trnddc04... : Idiot "Uncle Al" <UncleAl0@hate.spam.net> wrote in message : news:4656F9AF.4846BA46@hate.spam.net... : > hanson wrote: : http://groups.google.com/group/sci.physics/msg/59893aec79181fa8 : There are multitudes of known and commercially used : aliphatic- or aryl-nitro compounds, : say, RH + HNO3 --> R-NO2 + H2O. : >> : Are there also such organic Fluo-Nitrogen analogs, : say RH + NF3 --> R-NF2 + HF : >> : Are there also such organic Chlorate analogs, : say RH + HClO3 --> R-ClO2 + H2O, etc? : >> > : Does our NG rersident Nitro-man specialist, Prof. Donald : Haarmann have any info on their properties if they exist? : hanson : > : [Idiot Al] : > Idiot. A real man goes for RSF5 and aluminum or magnesium. : > : [hanson] : ahahaha... your beytsim must have fallen off and gummed up your : work if THAT is the answer from uncle Al, the severely gifted idiot. : Your ejaculate does not even address the question because you : have that certain uncertainty about your own masculinity which : seems to loom large on your idiot and Benzilated mind... ahahaha... : There must be too much aluminum in your brain, Al..... tzheimer. : My questions pertains to... well, you wouldn't understand, idiot : Thanks for the laughs, Schwartz... ahahaha.... : > : Now does anybody know?.. There must be more than just idiots like : Schwartz on the Usenet. : I can't answer your question, your knowledge of chemistry is much greater than mine. It would be stupid of me to try to guess, I don't have the expertise. I wouldn't be successful in animal husbandry either. Does that make me an idiot? I can support your view of Uncle Stooopid, though. That imbecile actually believes Einstein's crap, based on 1) Refereed journals. 2) Blind faith. 3) GPS works. It's a good thing Uncle Stooopid doesn't have a commercial pilot's license or he'd be landing 90 feet below the runway and damaging the lobsters flown in from Maine, that's how good GPS works. Damage to Uncle Stooopid would be non sequitur. Back to top   Ads Advertising Sponsor The_Man Guest Posted: Sat May 26, 2007 12:26 am    Post subject: Re: Organic NO2 analogs On May 25, 10:25 am, "hanson" <han...@quick.net> wrote: Quote: There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. That is the overall stoichiometry of the reaction, but you have left out something important. If you mix an aromatic compound with just nitric acid, you'll get something other than you expect. If you knew the mechanism for this reaction, it would help answer your questions below. Quote: Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF Think about the strength of sigma bonds formed between first row elements Quote: Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? Think about what stabilizes chlorine in positive oxidation states. Quote: Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson Back to top   Ads Advertising Sponsor hanson Guest Posted: Sat May 26, 2007 5:23 am    Post subject: Re: Organic NO2 analogs "The Dreidel" aka "The_Man" <me_so_horneeeee@yahoo.com> wrote in news:1180121185.128325.170310@w5g2000hsg.googlegroups.com... Quote: On May 25, 10:25 am, "hanson" <han...@quick.net> wrote: There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. [The Dreidel] That is the overall stoichiometry of the reaction, but you have left out something important. If you mix an aromatic compound with just nitric acid, you'll get something other than you expect. If you knew the mechanism for this reaction, it would help answer your questions below. [hanson] ..... "There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds"... So, your lamentations about mixing and expectation and reaction mechanisms are non issues since such production problems have been solved long ago... which is what is implied in my intro sentence above... ahaha.... Now listen, Dreidel, my question is directed at big boys and NOT to undergraduates who claim to have a PhD, post doc & an assured professorship, like you did here: http://groups.google.com/group/sci.physics/msg/510835821ae61ae9 http://groups.google.com/group/sci.physics/msg/f54f2f06b32374ab http://groups.google.com/group/comp.ai.philosophy/msg/9664b04338862277 < [ hanson] Quote: Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF [The Dreidel] Think about the strength of sigma bonds formed between first row elements [hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Fluo-Nitrogen analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [hanson] Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? [The Dreidel] Think about what stabilizes chlorine in positive oxidation states. [hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Chlorate analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [hanson] Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson [hanson to The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Back to top   Ads Advertising Sponsor The_Man Guest Posted: Sat May 26, 2007 8:17 pm    Post subject: Re: Organic NO2 analogs On May 25, 8:23 pm, "hanson" <han...@quick.net> wrote: Quote: "The Dreidel" aka "The_Man" <me_so_hornee...@yahoo.com> wrote innews:1180121185.128325.170310@w5g2000hsg.googlegroups.com...> On May 25, 10:25 am, "hanson" <han...@quick.net> wrote: There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. You asked what I thought was a serious question, and I tried to give you a serious answer. All you needed to do was look them up in the chemical databases. Once you find them, you won't understand much about the compounds of their chemistry. This is a topic studied in the beginning of the second semester of the sophmore for a chem, bio, or physics major. This is where most of the wannabe scientists get the hint that their real purpose in live is flipping hamburgers or sales. Evidently, you never even got this far. Quote: [The Dreidel] That is the overall stoichiometry of the reaction, but you have left out something important. If you mix an aromatic compound with just nitric acid, you'll get something other than you expect. If you knew the mechanism for this reaction, it would help answer your questions below. [hanson] .... "There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds"... So, your lamentations about mixing and expectation and reaction mechanisms are non issues since such production problems have been solved long ago... which is what is implied in my intro sentence above... ahaha.... Now listen, Dreidel, my question is directed at big boys and NOT to undergraduates who claim to have a PhD, post doc & an assured professorship, like you did here:http://groups.google.com/group/sci.physics/msg/510835821ae61ae9http://groups.google.com/group/sci.physics/msg/f54f2f06b32374abhttp://groups.google.com/group/comp.ai.philosophy/msg/9664b04338862277 [ hanson]>> Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> R-NF2 + HF [The Dreidel] Think about the strength of sigma bonds formed between first row elements [hanson] .. go ahead and do your thinking... but give me the answer to "Are there also such organic Fluo-Nitrogen analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... [hanson] Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? [The Dreidel] Think about what stabilizes chlorine in positive oxidation states. [hanson] .. go ahead and do your thinking... but give me the answer to "Are there also such organic Chlorate analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... [hanson] Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson [hanson to The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Back to top   Ads Advertising Sponsor Uncle Al Guest Posted: Sat May 26, 2007 10:52 pm    Post subject: Re: Organic NO2 analogs The_Man wrote: Quote: On May 25, 8:23 pm, "hanson" <han...@quick.net> wrote: "The Dreidel" aka "The_Man" <me_so_hornee...@yahoo.com> wrote innews:1180121185.128325.170310@w5g2000hsg.googlegroups.com...> On May 25, 10:25 am, "hanson" <han...@quick.net> wrote: There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. You asked what I thought was a serious question, and I tried to give you a serious answer. All you needed to do was look them up in the chemical databases. Once you find them, you won't understand much about the compounds of their chemistry. This is a topic studied in the beginning of the second semester of the sophmore for a chem, bio, or physics major. This is where most of the wannabe scientists get the hint that their real purpose in live is flipping hamburgers or sales. Evidently, you never even got this far. ahahahanson is the confluence of overwhelming ignorance with overweening arrogance. One wouldn't expect a freak crapping all over himself to be boring, but it is. -- Uncle Al http://www.mazepath.com/uncleal/ (Toxic URL! Unsafe for children and most mammals) http://www.mazepath.com/uncleal/lajos.htm#a2 Back to top   Ads Advertising Sponsor hanson Guest Posted: Sun May 27, 2007 10:05 am    Post subject: Re: Organic NO2 analogs AHAHAHA.. this is getting good now. I got me a mooch stuck on my fly-paper: (2) "The_ Dreidel" aka "The_Man" <me_so_horneeeee@yahoo.com> wrote in news:1180192663.196171.247080@q69g2000hsb.googlegroups.com... (1) "The_Dreidel" aka "The_Man" <me_so_horneeeee@yahoo.com> wrote in news:1180121185.128325.170310@w5g2000hsg.googlegroups.com... Quote: [orig-hanson] There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. [1-The Dreidel] That is the overall stoichiometry of the reaction, but you have left out something important. If you mix an aromatic compound with just nitric acid, you'll get something other than you expect. If you knew the mechanism for this reaction, it would help answer your questions below. [1- hanson] ..... "There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds"... So, your lamentations about mixing and expectation and reaction mechanisms are non issues since such production problems have been solved long ago... which is what is implied in my intro sentence above... ahaha.... Now listen, Dreidel, my question is directed at big boys and NOT to undergraduates who claim to have a PhD, post doc & an assured professorship, like you did here: http://groups.google.com/group/sci.physics/msg/510835821ae61ae9 http://groups.google.com/group/sci.physics/msg/f54f2f06b32374ab http://groups.google.com/group/comp.ai.philosophy/msg/9664b04338862277 < .... and so (2) The_ Dreidel aka "The_Man" <me_so_horneeeee@yahoo.com> keeps on digging his hole deeper with his incessant loud-mouth news:1180192663.196171.247080@q69g2000hsb.googlegroups.com... and keeps on whining about non-issues to my questions with Quote: [2 -The_ Dreidel] You asked what I thought was a serious question, and I tried to give you a serious answer. All you needed to do was look them up in the chemical databases. Once you find them, you won't understand much about the compounds of their chemistry. This is a topic studied in the beginning of the second semester of the sophmore for a chem, bio, or physics major. This is where most of the wannabe scientists get the hint that their real purpose in live is flipping hamburgers or sales. Evidently, you never even got this far. [2- hanson] ahahahaha..... Evidently, the loudmouthed Dreidel keeps on lamenting over an issue (nitration) that I did not ask for and he repeats himself but he has no useful answers to the pertinent questions below... ahahaha... .... barring his useless theory-advice above... ahahaha... So, Dreidel, your dilettante, semiprofound full-weaseling above is noted. Now answer the questions about properties of Fluoraminated R-NF2 and Oxochlorinated R-ClO2 compounds and spare me from and with your useless sideshow tripe. So, to help you.... Quote: [1- hanson repeats for the benefit of the The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Quote: [3- hanson] So, Dreidel, it is clear that you have not said anything useful nor intelligent... ahahaha... But keep on trying... One day there may be a "first" for you... ahahaha.... Thanks for the laughs, Dreidel Quote: [ 1- hanson ] Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> + HF [1- The Dreidel] Think about the strength of sigma bonds formed between first row elements [1- hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Fluo-Nitrogen analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [1- hanson] Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? [1- The Dreidel] Think about what stabilizes chlorine in positive oxidation states. [1- hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Chlorate analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [hanson -orig] Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson [1- hanson to The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Back to top   Ads Advertising Sponsor hanson Guest Posted: Sun May 27, 2007 10:07 am    Post subject: Re: Organic NO2 analogs AHAHAHA.. this is getting even better now. I got me two mooches stuck on my fly-paper... ahahaha... AHAHAHA... with "Uncle Al" <UncleAl0@hate.spam.net> coming out of this UrinAl to see what the buzz is all about in news:465873C8.AA1B049@hate.spam.net... wherein he admitted in a Freudian Slip that he... [drum roll]..... :: Alan Schwartz is the confluence of overwhelming ignorance with :: overweening arrogance. One wouldn't expect a freak crapping :: all over himself to be boring, but it is. Quote: (2) "The_ Dreidel" aka "The_Man" <me_so_horneeeee@yahoo.com> w/i news:1180192663.196171.247080@q69g2000hsb.googlegroups.com... (1) "The_Dreidel" aka "The_Man" <me_so_horneeeee@yahoo.com> w/i news:1180121185.128325.170310@w5g2000hsg.googlegroups.com... Quote: [orig-hanson] There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds, say, RH + HNO3 --> R-NO2 + H2O. [1-The Dreidel] That is the overall stoichiometry of the reaction, but you have left out something important. If you mix an aromatic compound with just nitric acid, you'll get something other than you expect. If you knew the mechanism for this reaction, it would help answer your questions below. [1- hanson] ..... "There are multitudes of known and commercially used aliphatic- or aryl-nitro compounds"... So, your lamentations about mixing and expectation and reaction mechanisms are non issues since such production problems have been solved long ago... which is what is implied in my intro sentence above... ahaha.... Now listen, Dreidel, my question is directed at big boys and NOT to undergraduates who claim to have a PhD, post doc & an assured professorship, like you did here: http://groups.google.com/group/sci.physics/msg/510835821ae61ae9 http://groups.google.com/group/sci.physics/msg/f54f2f06b32374ab http://groups.google.com/group/comp.ai.philosophy/msg/9664b04338862277 < .... and so (2) The_ Dreidel aka "The_Man" <me_so_horneeeee@yahoo.com> keeps on digging his hole deeper with his incessant loud-mouth news:1180192663.196171.247080@q69g2000hsb.googlegroups.com... and keeps on whining about non-issues to my questions with Quote: [2 -The_ Dreidel] You asked what I thought was a serious question, and I tried to give you a serious answer. All you needed to do was look them up in the chemical databases. Once you find them, you won't understand much about the compounds of their chemistry. This is a topic studied in the beginning of the second semester of the sophmore for a chem, bio, or physics major. This is where most of the wannabe scientists get the hint that their real purpose in live is flipping hamburgers or sales. Evidently, you never even got this far. [2- hanson] ahahahaha..... Evidently, the loudmouthed Dreidel keeps on lamenting over an issue (nitration) that I did not ask for and he repeats himself but he has no useful answers to the pertinent questions below... ahahaha... .... barring his useless theory-advice above... ahahaha... So, Dreidel, your dilettante, semiprofound full-weaseling above is noted. Now answer the questions about properties of Fluoraminated R-NF2 and Oxochlorinated R-ClO2 compounds and spare me from and with your useless sideshow tripe. So, to help you.... Quote: [1- hanson repeats for the benefit of the The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Quote: [3- hanson] So, Dreidel, it is clear that you have not said anything useful nor intelligent... ahahaha... But keep on trying... One day there may be a "first" for you... ahahaha.... Thanks for the laughs, Dreidel Quote: [ 1- hanson ] Are there also such organic Fluo-Nitrogen analogs, say RH + NF3 --> + HF [1- The Dreidel] Think about the strength of sigma bonds formed between first row elements [1- hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Fluo-Nitrogen analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [1- hanson] Are there also such organic Chlorate analogs, say RH + HClO3 --> R-ClO2 + H2O, etc? [1- The Dreidel] Think about what stabilizes chlorine in positive oxidation states. [1- hanson] ... go ahead and do your thinking... but give me the answer to "Are there also such organic Chlorate analogs" in existence, instead of your pathetic high school lamentations, by which you now are trying now to endear yourself to me. Don't be trying to impress me with your useless loud-mouthing. Say something useful and intelligent now.. and then we will see... ahahaha.... Quote: [hanson -orig] Does our NG rersident Nitro-man specialist, Prof. Donald Haarmann have any info on their properties if they exist? hanson [1- hanson to The Dreidel] THAT is what YOU should have answered to: "any info on their properties if they exist", instead of your pathetic and constant grandstanding and your sui-anointing yourself on my coat tails. ahaha... Now, remember, Dreidel, take heed,... I don't care if you remain "My_Fan", but realise, to me you are just a loud toy to have cyber fun with... so far... ahaha.. ahahaha... AHAHAHA... Now, try to say something useful & intelligent... For the first time. Thanks for the laughs, Dreidel ahahaha... ahahahanson Quote: [UrinAl pisses, hisses, kisses and misses] ahahahanson is the confluence of overwhelming ignorance with overweening arrogance. One wouldn't expect a freak crapping all over himself to be boring, but it is. [hanson] Idiot. (I am politely using here Uncle Al's standard form of his own greeting etiquette... Al's own patois so to speak)... .... AHAHAHA Idiot. Your 3-liner is much more convincing as a Freudian slip by / from you as it gives you (but not to the Dreidel) a "first", for you having confessed and characterized yourself eloquently that ::: Alan Schwartz is the confluence of overwhelming ignorance with ::: overweening arrogance. One wouldn't expect a freak crapping ::: all over himself to be boring, but it is. Quote: Al, it is too bad that you cranked yourself so needlessly... ahahaha.. because you do NOT have any answer neither, besides your gay sidestep-dance that "A real man goes for RSF5 and aluminum or magnesium"... ahahaha... You are forgiven for that, Al... because your attempt to console and suck up to the Dreidel is a second "first" for you, Al... You have finally shown mercy & compassion to someone.. even if it is a Dreidel... Keep that up, Al... That is much more productive and endearing then your usual advocacy to murder half of humankind. It's nice to see you getting soft in your waning years And as usual: Thanks for the laughs, Schwartz. ahahaha.... ahahahanson Quote: BTW, seriuosly for a moment. Forget Al, Mg and R-SF1,3 or-5. My issue has nothing to do with any pyrotechnics. We are looking into the situation if/whether R-NF2 or R-ClO2 compounds do have anti-neoplastic properties. I was hoping for a spark from a shot into the dark. But this is the Usenet.... ahahaha... ahahaha... Thanks for playing, though, dudes... Now let's go back to the regular cyber party with its hilarious 24/7 riots and laughs.... ahahaha.... Back to top   Ads Advertising Sponsor Uncle Al Guest Posted: Mon May 28, 2007 2:51 am    Post subject: Re: Organic NO2 analogs hanson wrote: Quote: AHAHAHA.. ahahaha... AHAHAHA... [snip] ahahahaha..... ahahaha... ahahaha... [snip] One wonders whether the spewing idiot has a copy-and-paste or types it out each time. Mostly likely types it. Quote: ahaha.. ahahaha... AHAHAHA... ahahaha... ahahahanson [snip] ahahaha... ahahaha.... [snip] ahahaha.... ahahaha.... [snip] Possibly fancies itself Jack Nicholson with green hair and lipstick. Quote: ahaha.. ahahaha... AHAHAHA... ahahaha... ahahahanson [snip] ahahahanson AHAHAHA ahahaha.. ahahaha... ahahaha.... ahahahanson [snip] ahahaha... ahahaha... ahahaha.... ahahahanson is the confluence of overwhelming ignorance with overweening arrogance. One wouldn't expect a freak crapping all over himself to be boring, but it is. -- Uncle Al http://www.mazepath.com/uncleal/ (Toxic URL! Unsafe for children and most mammals) http://www.mazepath.com/uncleal/lajos.htm#a2 Back to top   Ads Advertising Sponsor Androcles Guest Posted: Mon May 28, 2007 3:19 am    Post subject: Re: Organic NO2 analogs HAHAHA! Uncle Stooopid is fucked! "Uncle Al" <UncleAl0@hate.spam.net> wrote in message news:4659FD5C.8073DB5@hate.spam.net... : hanson wrote: : > : > AHAHAHA.. ahahaha... AHAHAHA... : [snip] : > ahahahaha..... ahahaha... ahahaha... : [snip] : [snop fat wert] ahahaha... AHAHAHA... : > ahahaha... ahahahanson : [snip] : > ahahaha... ahahaha.... : [snip] : > ahahaha.... : > ahahaha.... : [snip] : [snop fet wart] .. ahahaha... AHAHAHA... : > ahahaha... ahahahanson : [snip] : > > ahahahanson : > AHAHAHA : > ahahaha.. ahahaha... : > ahahaha.... ahahahanson : [snip] : > ahahaha... ahahaha... : > ahahaha.... : [snop illiterate river of shit (or as Dork would say, anip wet fart)] Back to top   Ads Advertising Sponsor Uncle Al Guest Posted: Mon May 28, 2007 5:38 am    Post subject: Re: Organic NO2 analogs Androcles wrote: Quote: HAHAHA! Uncle Stooopid is fucked! [snip carp] Hey Androclitty - are you still studying to improve your Apgar score? Even slum bunnies do better than a 3, certainly by the time hair grows in their pits. -- Uncle Al http://www.mazepath.com/uncleal/ (Toxic URL! Unsafe for children and most mammals) http://www.mazepath.com/uncleal/lajos.htm#a2 Back to top   Ads Advertising Sponsor Auriga Guest Posted: Mon May 28, 2007 8:37 am    Post subject: Re: Organic NO2 analogs Why don't you idiots crawl back under the rock you came out from. Stop polluting this forum with your senseless drivel. What a bunch of crap you spew. Take it somewhere else. Back to top   Ads Advertising Sponsor hanson Guest Posted: Mon May 28, 2007 10:10 am    Post subject: Re: Organic NO2 analogs ahaha..."Auriga" <bradash1@msn.com> cranked himself in message news:1180323456.538379.226890@k79g2000hse.googlegroups.com... Quote: Why don't you idiots crawl back under the rock you came out from. Stop polluting this forum with your senseless drivel. What a bunch of crap you spew. Take it somewhere else. [hanson] Well, my good fellow Brad, what we have here is a "failure in communications"... which is understandable in the glaring light of a certain poster who refers to himself as "uncle" and ... who eloquently characterizes himself, by his own words, by :: Alan Schwartz is the confluence of overwhelming ignorance with :: overweening arrogance. One wouldn't expect a freak crapping :: all over himself to be boring, but it is. Quote: Now, Brad, the situation that you so grievously are complaining about could be rectified if YOU were to show said "uncle" how to answer intelligently to the OP's initial request as stated in: http://groups.google.com/group/sci.chem/msg/59893aec79181fa8 that was followed up in another previous post with: My issue has nothing to do with any pyrotechnics. We are looking into the situation if/whether R-NF2 or R-ClO2 compounds do have anti-neoplastic properties. I was hoping for a spark from a shot into the dark. ---- But this is the Usenet.... with its sparkling "uncle Al"... ahahaha... ahahaha... hanson Back to top   Ads Advertising Sponsor Display posts from previous: All Posts1 Day7 Days2 Weeks1 Month3 Months6 Months1 Year Oldest FirstNewest First         Chemistry Talk Forum Index -> Chemistry Talk All times are GMT Goto page 1, 2  Next Page 1 of 2   Jump to: Select a forum Chemistry Talk----------------Chemistry Talk  You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You cannot vote in polls in this forum 97 Attacks blocked Powered by phpBB © 2001, 2005 phpBB Group