Weekly debugging of databases, found a suspicious rate coefficient. Rechecking NIST showed that it was a factor of 10 to high.
Adding rate rules for abstraction from butanal by HO2 and OH

Reference for Butanal + HO2
DOI: 10.1039/C2SC21090H
Updating H abstractions from branched alcohols by H and CH3

These values were updated by AVG, earlier values seem to be
suspiciously slow by factor of 10. SSM doesnt know why but
it could be related to error due to projection in CANTHERM.
Updating nBuOH + OH rate coefficients

Refitting the rate coefficients yo 3 parameter
using the 4 parameter fit  provided in Table 4 of
reference DOI: 10.1021/jp310910f
Adding rate rules for H abstraction from allylic sites of
alkenes by OH

The allylic site accounts for over 90% of H abstraction by OH
compared to the vinylic and methyl sites.
Estimating R. + O2 = Alkene + HO2 disproportionation rate
for alpha radical of alcohols.
Adding rate rule for O2 + vinyl = Alkyne + HO2 and O2 + secC-rad = diene +
HO2

The rate rule is derived from the estimate by Westbrook et al.
for C2H3 + O2 = C2H2 + HO2. This affects acetylene production
in many oxidation mechanism.

Also updating rate rule for O2 + allylic = diene + HO2
The estimate is based on secC-rad + O2 = Alkene + HO2 by accounting
for allylic stability (around + 7kcal/mol)
Commiting some changes to disproportionation reactions (mainly with O2) and H_Abstraction reactions (for alcohols) before pulling from master
Merge branch 'master' of https://github.com/GreenGroup/RMG-Java

Conflicts:
	databases/RMG_database/kinetics_groups/Disproportionation/rateLibrary.txt
	databases/RMG_database/kinetics_groups/H_Abstraction/tree.txt
Changed the addition of H to a primary double bond