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493\slmult0 \fs32\cf0\f0\charscalex100\b {HALOGENUROS DE ALQUILO}\b0
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\fs28\cf0\f2\charscalex100 {3.1.2 Propiedades f�sicas y qu�micas de los halogenuros
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\par\pard\li1120\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {Los halogenuros de
alquilo presentan propiedades similares a las de los
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incoloros, relativamente inodoros e insolubles en agua. Los puntos de ebullici�n de
los }\par\pard\li413\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100 {halogenuros de
alquilo se comportan de manera similar a }\fs22\cf0\f2\charscalex100
{lo}\fs22\cf0\f2\charscalex100 {s de los alcanos (a mayor
tama�o }\par\pard\li413\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100 {de cadena,
mayor punto de ebullici�n), estos van a ser mayores que en los alcanos por
las }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {interacciones
que presentan con el �tomo de hal�geno. }\par\pard\li1120\ri0\sl-213\slmult0
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400\slmult0 \fs22\cf0\f2\charscalex100 {De la misma forma, el tama�o del �tomo de
hal�geno tambi�n influye en el aumento de }\par\pard\li413\ri0\sl-413\slmult0
\fs24\cf0\f2\charscalex100 {los puntos de ebul ici�n y a mayor tama�o del �tomo de
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78� C }\par\pard\li666\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100
{- }\fs22\cf0\f2\charscalex100 {24}\fs22\cf0\f2\charscalex100 {�
C }\par\pard\li773\ri0\sl-426\slmult0 \fs22\cf0\f2\charscalex100 { 4�
C }\par\pard\li706\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100
{ }\fs22\cf0\f2\charscalex100 {42}\fs22\cf0\f2\charscalex100 {�
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\fs18\cf0\par\pard\li773\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li773\ri0\sl-
213\slmult0 \fs18\cf0\par\pard\li773\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li773\ri0\sl-360\slmult0 \fs18\cf3\f0\charscalex100\b {Fluoruro
de etilo }\b0 \par\pard\li986\ri0\sl-200\slmult0 \fs16\cf0\f0\charscalex100\b {p.e.
= }\b0 \fs16\cf0\f3\charscalex100 {\uc1\u61485X}\fs16\cf0\f0\charscalex100\b { 38�
C }\b0 \par\column\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-
213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-360\slmult0 \fs18\cf3\f0\charscalex100\b {Cloruro de
etilo}\b0 \par\pard\li240\ri0\sl-186\slmult0 \fs16\cf0\f0\charscalex100\b {p.e.
= }\b0 \fs16\cf0\f0\charscalex100\b {12}\b0 \fs16\cf0\f0\charscalex100\b {� C }\b0
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\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
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\fs18\cf3\f0\charscalex100\b {Bromuro de etilo}\b0 \par\pard\li293\ri0\sl-
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\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-253\slmult0
\fs18\cf3\f0\charscalex100\b {Yoduro de etilo}\b0 \par\pard\li226\ri0\sl-
213\slmult0 \fs16\cf0\f0\charscalex100\b {p.e. = }\b0 \fs16\cf0\f0\charscalex100\b
{72}\b0 \fs16\cf0\f0\charscalex100\b {� C }\b0
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i1120\ri0\sl-293\slmult0 \fs24\cf0\f2\charscalex100 {En estas representaciones se
observa que el �tomo de hal�geno (que est� }\par\pard\li413\ri0\sl-
413\slmult0 \fs24\cf0\f2\charscalex100 {representado por las esferas de color
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413\slmult0 \fs24\cf0\f2\charscalex100 {cada mol�cula), incrementa su tama�o en el
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400\slmult0 \fs22\cf0\f2\charscalex100 {La }\fs22\cf0\f2\charscalex100 { mayor�a de
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densos }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {que el agua.
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1}}}}\pgwsxn12240\pghsxn15840\marglsxn666\margrsxn133\margtsxn666\margbsxn413\pard\
li413\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li413\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li413\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li413\ri0\sl-
213\slmult0 \fs18\cf0\par\pard\li413\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li413\ri0\sl-426\slmult0 \fs28\cf0\f2\charscalex100 {3.1.2.3
Con reactivo de Grignard}\par\pard\li1120\ri0\sl-453\slmult0
\fs24\cf0\f2\charscalex100 {Los halogenuros de alquilo, reaccionan con el magnesio
met�lico en disoluci�n de �ter }\par\pard\li413\ri0\sl-413\slmult0
\fs22\cf0\f2\charscalex100 {para formar compuestos organomet�licos de f�rmula
general }{ }\fs22\cf0\f0\charscalex100\b {R}\b0 \fs22\cf0\f0\charscalex100\b
{\uc1\u8211X}\b0 \fs22\cf0\f0\charscalex100\b {X}\b0 \fs22\cf0\f0\charscalex100\b
{\uc1\u8211X}\b0 \fs22\cf0\f0\charscalex100\b {Mg}\b0 \fs22\cf0\f2\charscalex100 {,
los hal�genos pueden }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100
{ser I, Br, Cl. Los cloruros son menos reactivos que los bromuros y los yoduros,
mientras que }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {los
fluoruros org�nicos casi no reaccionan con el magnesio.
Ejemplo: }\par\pard\sect\sectd\sbknone\pgwsxn12240\pghsxn15840\marglsxn666\margrsxn
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\*\tx3320\fs22\cf0\f2\charscalex100 {H}{\sub \fs18\cf0\f2\charscalex100
{3}}\fs22\cf0\f2\charscalex100 {C}\tab \fs22\cf0\f2\charscalex100 {CH}{\sub
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\fs18\cf0\par\pard\li53\ri0\sl-440\slmult0 \fs22\cf10\f2\charscalex100
{Mg}\par\pard\li0\ri0\sl-306\slmult0 \fs22\cf0\f4\charscalex100
{�ter}\par\column\pard\li866\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li866\ri0\sl-
266\slmult0 \fs22\cf10\f2\charscalex100 {Mg}\fs22\cf9\f2\charscalex100
{Br}\par\pard\li80\ri0\sl-400\slmult0 \*\tx626\fs22\cf0\f2\charscalex100 {H}
{\sub \fs18\cf0\f2\charscalex100 {3}}\fs22\cf0\f2\charscalex100 {C}\tab
\fs22\cf0\f2\charscalex100 {CH}{\sub \fs18\cf0\f2\charscalex100
{2}}\fs22\cf0\f2\charscalex100 {CH CH}{\sub \fs18\cf0\f2\charscalex100
{3}}\par\pard\li0\ri0\sl-253\slmult0 \fs22\cf8\f2\charscalex100 {Reactivo de
Grignard}\par\pard\sect\sectd\sbknone\pgwsxn12240\pghsxn15840\marglsxn666\margrsxn1
33\pard\li1120\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li1120\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li1120\ri0\sl-373\slmult0 \fs24\cf0\f2\charscalex100 {La
aplicaci�n del reactivo de Grignard es en la s�ntesis de compuestos org�nicos
como }\par\pard\li413\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100 {alcoholes y
cetonas. Y es tambi�n una herramienta importante en la formaci�n de
enlaces }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100
{carbono }\fs24\cf0\f4\charscalex100 {\uc1\u8211X}\fs24\cf0\f2\charscalex100
{ carbono para la s�ntesis de diversos compuestos
org�nicos. }\par\pard\li413\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li413\ri0\sl-
213\slmult0 \fs18\cf0\par\pard\li413\ri0\sl-440\slmult0 \fs28\cf0\f2\charscalex100
{3.1.2.3 M�todos de obtenci�n: Halogenaci�n de alcanos.}\par\pard\li1120\ri0\sl-
453\slmult0 \fs22\cf0\f2\charscalex100 {Podemos obtener halogenuros de alquilo a
partir de alcanos, haciendo reaccionar al }\par\pard\li413\ri0\sl-426\slmult0
\fs24\cf0\f2\charscalex100 {alcano con Cl}{\sub \fs16\cf0\f2\charscalex100
{2}}\fs24\cf0\f2\charscalex100 {, o Br}{\sub \fs16\cf0\f2\charscalex100
{2}}\fs24\cf0\f2\charscalex100 { por medio de una reacci�n de radicales
libres. Para poder reaccionar}\par\pard\li413\ri0\sl-400\slmult0
\fs24\cf0\f2\charscalex100 {estos hal�genos con el alcano, se
requiere }\fs24\cf0\f2\charscalex100 {de }\fs24\cf0\f2\charscalex100 {la
presencia de luz ultravioleta (hu) para la }\par\pard\li413\ri0\sl-
413\slmult0 \fs24\cf0\f2\charscalex100 {formaci�n del haloalcano.
Ejemplo: }\par\pard\li2840\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li2840\ri0\sl-
320\slmult0 \fs26\cf0\f2\charscalex100
{hu}\par\pard\sect\sectd\sbknone\pgwsxn12240\pghsxn15840\marglsxn666\margrsxn133\co
ls4\colno1\colw3586\colsr-0\colno2\colw1466\colsr-0\colno3\colw2986\colsr-
0\colno4\colw3400\pard\li1613\ri0\sl-453\slmult0 \fs22\cf0\f2\charscalex100 {CH}
{\sub \fs16\cf0\f2\charscalex100 {4}}\fs38\cf0\f2\charscalex100 {+}
{ }\fs22\cf11\f2\charscalex100 {Cl}{\sub \fs16\cf11\f2\charscalex100
{2}}\par\column\pard\li0\ri0\sl-453\slmult0 \*\tx533\fs22\cf0\f2\charscalex100 {H}
{\sub \fs16\cf0\f2\charscalex100 {3}}\fs22\cf0\f2\charscalex100 {C}\tab
\fs22\cf11\f2\charscalex100 {Cl}\fs38\cf0\f2\charscalex100 {+}
{ }\fs22\cf0\f2\charscalex100 {H}\fs22\cf11\f2\charscalex100
{Cl}\par\pard\li680\ri0\sl-293\slmult0 \fs22\cf10\f2\charscalex100 {Cl}{\sub
\fs14\cf10\f2\charscalex100 {2}}\par\column\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-533\slmult0
\fs22\cf0\f2\charscalex100 {CH}{\sub \fs16\cf0\f2\charscalex100
{2}}\fs22\cf11\f2\charscalex100 {Cl}{\sub \fs16\cf11\f2\charscalex100
{2}}\fs38\cf0\f2\charscalex100 {+}{ }\fs22\cf0\f2\charscalex100
{H}\fs22\cf11\f2\charscalex100 {Cl}\par\pard\li693\ri0\sl-386\slmult0
\fs22\cf10\f2\charscalex100 {Cl}{\sub \fs14\cf10\f2\charscalex100
{2}}\par\pard\li1466\ri0\sl-453\slmult0 \*\tx1906\fs22\cf0\f2\charscalex100
{CH}\tab \fs22\cf11\f2\charscalex100 {Cl}{\sub \fs16\cf11\f2\charscalex100
{3}}\fs38\cf0\f2\charscalex100 {+}{ }\fs22\cf0\f2\charscalex100
{H}\fs22\cf11\f2\charscalex100 {Cl}\par\pard\li2160\ri0\sl-306\slmult0
\fs22\cf10\f2\charscalex100 {Cl}{\sub \fs14\cf10\f2\charscalex100
{2}}\par\column\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-
213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li0\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li0\ri0\sl-560\slmult0
\*\tx280\fs22\cf0\f2\charscalex100 {C}\tab \fs22\cf11\f2\charscalex100 {Cl}{\sub
\fs16\cf11\f2\charscalex100 {4}}\fs38\cf0\f2\charscalex100 {+}
{ }\fs22\cf0\f2\charscalex100 {H}\fs22\cf11\f2\charscalex100
{Cl}\par\pard\sect\sectd\sbknone\pgwsxn12240\pghsxn15840\marglsxn666\margrsxn133\pa
rd\li1120\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li1120\ri0\sl-213\slmult0
\fs18\cf0\par\pard\li1120\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li1120\ri0\sl-
293\slmult0 \fs24\cf0\f2\charscalex100 {La }\fs24\cf0\f2\charscalex100
{halogenaci�n de alcanos no es un m�todo adecuado para la s�ntesis de
halogenuros }\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100
{de }\fs24\cf0\f2\charscalex100 {alquilo, ya que como vemos en la reacci�n
anterior, obtenemos una mezcla de compuestos }\par\pard\li413\ri0\sl-413\slmult0
\fs24\cf0\f2\charscalex100 {halogenados, ya que la reacci�n continua hasta obtener
una mezcla de productos, mono-, di-}\fs24\cf0\f2\charscalex100
{,}\par\pard\li413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {tri- y tetra-
clorados. }\par\pard\sect\sectd\sbknone\pgwsxn12240\pghsxn15840\marglsxn666\margrsx
n133\pard\sect\sectd\sbkpage{\shp
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}}}}{\shp
{\*\shpinst
\shpleft9893\shptop10706\shpright11066\shpbottom11960
\shpfhdr0\shpwr3\shpwrk0\shpfblwtxt1\shplid2163\shpz24\shpbxpage\shpbypage
\absh15840\absw12240{\sp{\sn shapeType}{\sv 75}}
{\sp{\sn fFlipH}{\sv 0}}
{\sp{\sn fFlipV}{\sv 0}}
{\sp{\sn pibFlags}{\sv 2}}
{\sp{\sn fLine}{\sv 0}}{\sp{\sn fEditedWrap}{\sv 0}}
{\sp{\sn fBehindDocument}{\sv 1}}
{\sp{\sn pib}{\sv {\pict
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}}}}
{\shp{\*\shpinst\shpleft9906\shptop9533\shpright11040\shpbottom10733\shpfhdr0\shpwr
3\shpwrk0\shpfblwtxt1\shplid2141\shpz25\shpbxpage\shpbypage
{\sp{\sn shapeType}{\sv 0}}
{\sp{\sn fFlipH}{\sv 0}}
{\sp{\sn fFlipV}{\sv 0}}
{\sp{\sn rotation}{\sv 0}}
{\sp{\sn geoRight}{\sv 1134}}
{\sp{\sn geoBottom}{\sv 1200}}
{\sp{\sn shapePath}{\sv 4}}
{\sp{\sn pVerticies}{\sv 8;171;(0,93);(0,93);(0,80);(0,80);(0,66);(13,53);(13,53);
(13,40);(13,40);(26,40);(26,26);(40,26);(40,13);(40,13);(53,13);(53,13);(66,0);
(80,0);(80,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);
(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);(93,0);
(93,0);(93,0);(93,0);(1040,0);(1040,0);(1040,0);(1053,0);(1066,0);(1066,0);
(1080,13);(1080,13);(1093,13);(1093,13);(1106,26);(1106,26);(1106,40);(1120,40);
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(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);
(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);
(1133,93);(1133,93);(1133,93);(1133,93);(1133,93);(1133,1106);(1133,1106);
(1133,1106);(1133,1120);(1133,1120);(1133,1133);(1133,1146);(1120,1146);
(1120,1160);(1120,1160);(1106,1160);(1106,1173);(1106,1173);(1093,1186);
(1093,1186);(1080,1186);(1080,1186);(1066,1200);(1066,1200);(1053,1200);
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(1040,1200);(1040,1200);(1040,1200);(1040,1200);(1040,1200);(1040,1200);
(1040,1200);(1040,1200);(1040,1200);(1040,1200);(1040,1200);(93,1200);(93,1200);
(93,1200);(80,1200);(80,1200);(66,1200);(53,1186);(53,1186);(40,1186);(40,1186);
(40,1173);(26,1173);(26,1160);(13,1160);(13,1160);(13,1146);(13,1146);(0,1133);
(0,1120);(0,1120);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);
(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);
(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,1106);(0,93);}}
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{\sp{\sn fFillOK}{\sv 1}}
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{\sp{\sn fillColor}{\sv 15527148}}
{\sp{\sn fLine}{\sv 0}}{\sp{\sn lineColor}{\sv 0}}
{\sp{\sn lineType}{\sv 0}}
{\sp{\sn fArrowheadsOK}{\sv 0}}
{\sp{\sn fBehindDocument}{\sv 1}}
{\sp{\sn fLayoutInCell}{\sv 1}}}}{\shp
{\*\shpinst
\shpleft8773\shptop9533\shpright9906\shpbottom10733
\shpfhdr0\shpwr3\shpwrk0\shpfblwtxt1\shplid2164\shpz26\shpbxpage\shpbypage
\absh15840\absw12240{\sp{\sn shapeType}{\sv 75}}
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{\sp{\sn pibFlags}{\sv 2}}
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\fs18\cf0\par\pard\li413\ri0\sl-426\slmult0 \fs28\cf0\f2\charscalex100 {3.1.3 Usos
y aplicaciones}\par\pard\li1120\ri0\sl-453\slmult0 \fs24\cf0\f2\charscalex100 {Los
halogenuros de alquilo tienen diversas aplicaciones entre las cuales
est�n: }\par\pard\li773\ri0\sl-213\slmult0 \fs18\cf0\par\pard\li773\ri0\sl-
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{a)}\fs24\cf0\f2\charscalex100 { }{ }\fs24\cf0\f0\charscalex100\i {Disolventes.}\i0
\fs24\cf0\f2\charscalex100 { Los haluros de alquilo se utilizan principalmente
como }\par\pard\li1133\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {disolventes
industriales, se utilizan en diversas industrias como
la }\par\pard\li3080\ri0\sl-413\slmult0
\*\tx4560\*\tx7106\fs24\cf0\f2\charscalex100 {electr�nica }\tab
\fs24\cf0\f2\charscalex100 {para la limpieza }\tab \fs24\cf0\f2\charscalex100 {de
componentes }\par\pard\li3080\ri0\sl-413\slmult0 \fs24\cf0\f4\charscalex100
{electr�nicos y chip\uc1\u8217Xs, en la limpieza en seco de
prendas, }\par\pard\li3080\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {solventes
de pinturas, etc. }\par\pard\li3080\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100
{Entre los m�s utilizados est�n el tricloroetileno }\par\pard\li3080\ri0\sl-
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{d)}\i0 \fs24\cf0\f0\charscalex100\i { Refrigerantes.}\i0
\fs24\cf0\f2\charscalex100 { Fluoroalcanos tambi�n conocidos como }
{ }\fs24\cf0\f0\charscalex100\i {freones}\i0 \fs24\cf0\f2\charscalex100
{ }\fs24\cf0\f2\charscalex100 {o}\tab \fs24\cf0\f0\charscalex100\i
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{sustituir al amoniaco como gas refrigerante. El
fre�n-}\fs24\cf0\f2\charscalex100 {12}\fs16\cf0\f3\charscalex100
{\uc1\u61666X}\fs24\cf0\f2\charscalex100 { (CCl}{\sub \fs16\cf0\f2\charscalex100
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\fs24\cf0\f2\charscalex100 {fue de los primeros en utilizarse como
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\*\tx5026\*\tx5733\*\tx6413\fs24\cf0\f2\charscalex100 {reemplazados}\tab
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y}\par\pard\li3413\ri0\sl-413\slmult0 \fs24\cf0\f2\charscalex100 {pesticidas. En
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sin embargo }\par\pard\li3413\ri0\sl-413\slmult0 \fs22\cf0\f2\charscalex100 {debido
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\fs24\cf0\f0\charscalex100\b {Referencias }\b0 \par\pard\li413\ri0\sl-
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{Jr., L. W. (2004). }\fs24\cf0\f0\charscalex100\i {Qu�mica Org�nica.}\i0
\fs24\cf0\f2\charscalex100 { Pearson-Prentice Hall. }\par\pard\li413\ri0\sl-
280\slmult0 \fs24\cf0\f2\charscalex100 {McMURRY, J.
(2001). }\fs24\cf0\f0\charscalex100\i {Qu�mica Org�nica.}\i0
\fs24\cf0\f2\charscalex100 { International Thomson. }\par\pard\li413\ri0\sl-
280\slmult0 \fs24\cf0\f2\charscalex100 {SALOMONS, T. G.
(1996). }\fs24\cf0\f0\charscalex100\i {Fundamentals of Organic Chemistry.}\i0
\fs24\cf0\f2\charscalex100 { Wiley. }\par\pard\li413\ri0\sl-266\slmult0
\fs24\cf0\f0\charscalex100\i {WIKIPEDIA}\i0 \fs24\cf0\f2\charscalex100 {.
(17 }\fs24\cf0\f2\charscalex100 {de}\fs24\cf0\f2\charscalex100 { Junio de 2010).
Recuperado el 22 de Febrero de 2010, de WIKIPEDIA: }\par\pard\li413\ri0\sl-
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{http://en.wikipedia.org/wiki/Haloalkane }\par}