INTERRELATIONS OF THE ENERGETICS OF AMIDES AND ALKENES - ENTHALPIES OF FORMATION OF N,N-DIMETHYL DERIVATIVES OF PIVALAMIDE, 1-ADAMANTYLCARBOXAMIDE AND BENZAMIDE, AND OF STYRENE AND ITS ALPHA-METHYLATED, TRANS-BETA-METHYLATED AND BETA,BETA-METHYLATED DERIVATIVES
Jlm. Abboud et al., INTERRELATIONS OF THE ENERGETICS OF AMIDES AND ALKENES - ENTHALPIES OF FORMATION OF N,N-DIMETHYL DERIVATIVES OF PIVALAMIDE, 1-ADAMANTYLCARBOXAMIDE AND BENZAMIDE, AND OF STYRENE AND ITS ALPHA-METHYLATED, TRANS-BETA-METHYLATED AND BETA,BETA-METHYLATED DERIVATIVES, Journal of physical organic chemistry, 8(1), 1995, pp. 15-25
The enthalpies of formation of the condensed phase and gaseous N,N-dim
ethyl derivatives of pivalamide, 1-adamantylcarboxamide and benzamide
were determined by combustion calorimetry and the associated enthalpie
s of vaporization and sublimation. The enthalpies of formation of styr
ene and its alpha-, trans-beta- and beta,beta-methylated derivatives w
ere determined from measurements of their enthalpies of hydrogenation
in dilute hydrocarbon solution. Strain and resonance effects of amides
and alkenes are discussed in terms of the exo-/endothermicity of the
following reactions: CH3CONH2(g) + RC(CH3)=CH2 --> (CH3)2C=CH2(g) + RC
ONH2(g) CH3CON(CH3)2(g) + RCH=C(CH3)2(g) --> CH3CH=C(CH3)2(g) + RCON(C
H3)2(g) and in terms of the difference of enthalpies of formation of t
he isomeric (Z)- and (E)-RCH=CHCH3.