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{\bf Table VII}. Proton affinities in kcal/mol}
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\begin{tabular*}{10in}[t]{lllllllllll}
\hline
\multicolumn{1}{c}{Molecule} &
\multicolumn{1}{c}{RHF/6d\footnote{See footnotes in Table I and V 
for method description.}} &
\multicolumn{1}{c}{MP2/6d} &
\multicolumn{1}{c}{RHF/5d} &
\multicolumn{1}{c}{MP2/5d} &
\multicolumn{1}{c}{DMol} &
\multicolumn{1}{c}{DG/L} &
\multicolumn{1}{c}{DG/N)} &
\multicolumn{1}{c}{DN/L} &
\multicolumn{1}{c}{DN/N} &
\multicolumn{1}{c}{Exp.} \\
\hline
CH$_3$CH$_2$OH & 190.56(2.3\footnotemark[2]\footnotetext[2]{Deviation from experiment $P(A)_{calc.} - P(A)_{exp.}$})
& 187.54($-$0.8) & 190.56(2.3) & 187.59($-$0.7) & 176.72($-$11.6) & 180.28($-$8.0) & 185.07($-$3.2) & 179.99($-$8.3) & 185.35($-$3.0) 
 &  188.3\footnotemark[3]\footnotetext[3]{Experimental data from ref. 34.} \\
HCOO$^-$ & 353.88(8.7)\footnotemark[4]\footnotetext[4]{348.96(3.8) for DZ6D$^{(+)}$ basis set)}
 & 351.72(6.5)\footnotemark[5]\footnotetext[5]{343.42($-$1.8) for DZ6D$^{(+)}$ basis set)}
 & 354.03(8.8) & 351.81(6.6) & 334.75($-$10.5) & 340.46($-$4.7) & 345.75(0.5) & 340.10($-$5.1) & 345.67(0.5) 
&  345.2\footnotemark[6]\footnotetext[6]{Experimental data from ref. 41.}  \\
HCOOH & 182.99(4.2) & 176.94($-$1.9) & 183.04(4.2) & 176.95($-$1.9) & 167.29($-$11.5) & 172.16($-$6.6)
& 176.83($-$2.0) &172.57($-$6.2)& 176.76($-$2.0)
      &  178.8\footnotemark[3] \\
CH$_3$OH & 185.34(3.4) & 182.74(0.8) & 185.33(3.4) & 182.78(0.9) & 170.07($-$11.8) & 174.61($-$7.3)
 & 178.98($-$2.9)   &174.32($-$7.6) & 179.24($-$2.7)
   &  181.9\footnotemark[3] \\
CH$_3$NH$_2$ & 219.27(5.2) & 218.54(4.4) & 219.21(5.1) & 218.59(4.5) & 205.25($-$8.8) & 209.69($-$4.4)
 & 214.57(0.5)  &209.42($-$4.7) & 214.37(0.3)
    &  214.1\footnotemark[3] \\
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