Table 3. Determined Molar HOM Yields Using NO₃^– Ionization.

compound	total yield (%)	due to O3 (%)	due to OH (%)a	ref
isoprene	4b	0.01 ± 0.005	0.03 ± 0.015	Jokinen et al. 2015100
				Ng et al. 2008147
cyclopentene	4.8 ± 0.2			Berndt et al. 201545
cyclohexene	4 ± 2			Ehn et al. 20145
	4.5 ± 3.8			Rissanen et al. 201482
	6.0 ± 0.1 (7.3 ± 0.2)c			Berndt et al. 201545
cycloheptene	5.9 ± 0.1			Berndt et al. 201545
cyclooctene	5.9 ± 0.1			Berndt et al. 201545
α-pinene	7.0 ± 3.5			Ehn et al. 20145
	3.4 ± 1.0	3.4 ± 1.7	0.44 ± 0.22	Jokinen et al. 2015100
		1.2 (+1.2/–0.72)	1.2 (+1.2/–0.72)	Kirkby et al. 201683
limonene	17.0 ± 8.5	5.3 ± 2.7	0.93 ± 0.47	Ehn et al. 20145
				Jokinen et al. 2015100
β-pinene	<0.1	0.12 ± 0.06	0.58 ± 0.29	Ehn et al. 20145
				Jokinen et al. 2015100
myrcene		0.47 ± 0.29	0.14 ± 0.07	Jokinen et al. 2015100
β-caryophyllene	1.7 ± 1.28			Jokinen et al. 2016134
	0.5 ± 0.3			Richters et al. 2016170
	1.8 ± 0.9c			Richters et al. 2016170
α-cedrene	0.6 ± 0.3			Richters et al. 2016170
	0.6 ± 0.3c
α-humulene	1.4 ± 0.7			Richters et al. 2016170
benzene			0.2d	Molteni et al. 201885
toluene			0.1d	Molteni et al. 201885
ethylbenzene			0.2d	Molteni et al. 201885
(o/m/p)-xylene			1.0–1.7d	Molteni et al. 201885
mesitylene			0.6d	Molteni et al. 201885
naphthalene			1.8d	Molteni et al. 201885
biphenyl			2.5d	Molteni et al. 201885

^aDeduced by using an OH scavenger in an ozonolysis experiment.

^bDetermined using CF₃O^– ionization.

^cDetermined using acetate ionization.

^dPure OH experiments. Note that almost all the experiments have been done at room temperature 20 ± 5 °C.