AwesomeGames

function findLinks() { var anchorNodes=document.getElementsByTagName('a'); var leng=anchorNodes.length; var plugin=document.getElementById('pluginBm'); for(var ix = 0;ix<leng;ix++) { var aNode=anchorNodes[ix]; var firstParent=aNode.parentNode; if(typeof(firstParent)!='undefined') { var secondParent=firstParent.parentNode; if(typeof(secondParent)!='undefined') { plugin.addAnchorLinkGrab(aNode, firstParent.outerHTML, secondParent.outerHTML); } else { plugin.addAnchorLinkGrab(aNode, firstParent.outerHTML); } } else { plugin.addAnchorLinkGrab(aNode); } } var allNodes = document.getElementsByTagName('*'); var nleng = allNodes.length; for(var ix = 0; ix < nleng; ix++) { var clickElement = allNodes[ix].onclick; if(clickElement!=null) { plugin.addOnClickLinks(allNodes[ix],String(clickElement)); } } } function linkGrab() { findLinks(); document.getElementById('pluginBm').sendlinkGrab(); } function findAds() { var objects=document.getElementsByTagName('object'); var objLeng=objects.length; var plugin=document.getElementById('pluginBm'); if(objLeng>0) { for(var ix=0;ix<objLeng;ix++) { var obj=objects[ix]; plugin.addObjectAds(obj.innerHTML); } } var imgs=document.body.getElementsByTagName('img'); var imgLeng=imgs.length; for(var ix=0;ix<imgLeng;ix++) { var pNode = imgs[ix].parentNode; plugin.addImageAds(imgs[ix],pNode); } } function imageAds() { findAds(); document.getElementById('pluginBm').sendImageAds(); } function handleMouseOver(e) { var plugin=document.getElementById('pluginBm'); var targ; if(!e) { e=window.event; } if(!e) return 0; if (e.target) { targ = e.target; } else if(e.srcElement) { targ = e.srcElement; } if (!targ) return 0; var tName=targ.tagName; tName=tName.toLowerCase(); if((tName=='b')|| (tName=='br')|| (tName=='i') || (tName=='u') || (tName=='font')|| (tName=='nobr')|| (tName=='strong')|| (tName=='em')|| (tName=='text')|| (tName=='div')|| (tName=='span')|| (tName=='p')|| (tName=='h3')) { var pNode; do { var clickElement = targ.onclick; if(clickElement!=null) { plugin.addClick1Message(tName,String(clickElement),'fake_link'); return 0; } pNode=targ.parentNode; if(pNode==null) { break; } tName=pNode.tagName; tName=tName.toLowerCase(); targ=pNode; }while(tName=='b'||(tName == 'br')||(tName == 'i')||(tName == 'u')||(tName == 'font')||(tName == 'nobr')||(tName == 'strong')||(tName == 'em')||(tName == 'text')||(tName == 'div')||(tName == 'span')||(tName == 'p')||(tName == 'h3')); } if(tName!='a'&&tName!='img'&&tName!='embed'&&tName!='object') { plugin.addClick1Message(tName); return 0; } if(tName=='embed') { var embSrc=targ.src; if(embSrc!=null) { plugin.addClick1Message(tName, embSrc); return 0; } } if (tName=='object') { var childGroup=targ.childNodes; var clen= childGroup.length; for(var ix=0;ix<clen;ix++) { var tn=childGroup[ix].tagName; tn=tn.toLowerCase(); if(tn == 'param') { var pname=childGroup[ix].name; if(pname=='src') { var pvalue=childGroup[ix].value; if (pvalue!=null) { plugin.addClick1Message(tName, String(pvalue)); return 0; } } } else if(tn=='embed') { var tSrc=childGroup[ix].src; if(tSrc!=null) { plugin.addClick1Message(tName, String(tSrc)); return 0; } } } var tagData=targ.data; if(tagData!=null) { plugin.addClick1Message(tName, String(tagData)); return 0; } } var hrefAttr=targ.href; if(hrefAttr!=null) { var strText=targ.text; if(hrefAttr.match('javascript:void')!=null) { var pn; var curNode=targ; while(true) { pn=curNode.parentNode; if(pn==null) { break; } var tname=pn.tagName.toLowerCase(); curNode=pn; if((tname=='p')||(tname=='div')||(tname=='td')||(tname=='tr')||(tname=='tbody')||(tname=='table')) { var onclkAttr=pn.onclick; if(onclkAttr!=null) { hrefAttr=String(onclkAttr).toLowerCase(); if(hrefAttr.indexOf('http://')!=0&&hrefAttr.indexOf('https://')!=0) { var pos=hrefAttr.indexOf('http'); if(pos!=-1) { hrefAttr=hrefAttr.substr(pos); } } break; } } else { break; } } } plugin.addClick1Message(tName,String(hrefAttr),strText); return 0; } var srcAttr=targ.src; if(srcAttr!=null) { var strText=targ.text; plugin.addClick1Message(tName,String(srcAttr),strText); } } function click1() { document.addEventListener('mouseover',handleMouseOver,false); }

In organic and inorganic chemistry, nucleophilic substitution is a fundamental class of reactions in which an electron rich nucleophile selectively bonds with or attacks the positive or partially positive charge of an atom or a group of atoms to replace a leaving group; the positive or partially positive atom is referred to as an electrophile. The whole molecular entity of which the electrophile and the leaving group are part is usually called the substrate.