Input interpretation
2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone
Basic properties
molar mass | 322 g/mol formula | C_10H_10Br_2O_2 empirical formula | Br_C_5O_H_5 SMILES identifier | CC(C)C1=C(C(=O)C(=C(C1=O)Br)C)Br InChI identifier | InChI=1/C10H10Br2O2/c1-4(2)6-8(12)9(13)5(3)7(11)10(6)14/h4H, 1-3H3 InChI key | GHHZELQYJPWSMG-UHFFFAOYSA-N
Lewis structure
Draw the Lewis structure of 2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone. Start by drawing the overall structure of the molecule, ignoring potential double and triple bonds: Count the total valence electrons of the bromine (n_Br, val = 7), carbon (n_C, val = 4), hydrogen (n_H, val = 1), and oxygen (n_O, val = 6) atoms: 2 n_Br, val + 10 n_C, val + 10 n_H, val + 2 n_O, val = 76 Calculate the number of electrons needed to completely fill the valence shells for bromine (n_Br, full = 8), carbon (n_C, full = 8), hydrogen (n_H, full = 2), and oxygen (n_O, full = 8): 2 n_Br, full + 10 n_C, full + 10 n_H, full + 2 n_O, full = 132 Subtracting these two numbers shows that 132 - 76 = 56 bonding electrons are needed. Each bond has two electrons, so in addition to the 24 bonds already present in the diagram add 4 bonds. To minimize formal charge carbon wants 4 bonds and oxygen wants 2 bonds. Identify the atoms that want additional bonds and the number of electrons remaining on each atom: Fill in the 4 bonds by pairing electrons between adjacent highlighted atoms: Answer: | |
Estimated thermodynamic properties
melting point | 233.6 °C boiling point | 465 °C critical temperature | 1002 K critical pressure | 3.412 MPa critical volume | 633.5 cm^3/mol molar heat of vaporization | 62.8 kJ/mol molar heat of fusion | 19.37 kJ/mol molar enthalpy | -333.4 kJ/mol molar free energy | -132.1 kJ/mol (computed using the Joback method)
Units
Quantitative molecular descriptors
longest chain length | 7 atoms longest straight chain length | 3 atoms longest aliphatic chain length | 3 atoms aromatic atom count | 0 atoms H-bond acceptor count | 2 atoms H-bond donor count | 0 atoms
Elemental composition
Find the elemental composition for 2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone in terms of the atom and mass percents: atom percent = N_i/N_atoms × 100% mass percent = (N_im_i)/m × 100% Plan: • Write the chemical formula and gather atomic masses from the periodic table. • Determine values for N_i, m_i, N_atoms and m using these items. • Finally, compute the percents and check the results. Write the chemical formula: C_10H_10Br_2O_2 Use the chemical formula, C_10H_10Br_2O_2, to count the number of atoms, N_i, for each element and find the total number of atoms, N_atoms: | number of atoms Br (bromine) | 2 C (carbon) | 10 O (oxygen) | 2 H (hydrogen) | 10 N_atoms = 2 + 10 + 2 + 10 = 24 Divide each N_i by N_atoms to calculate atom fractions. Then use the property that atom fractions must sum to one to check the work: | number of atoms | atom fraction Br (bromine) | 2 | 2/24 C (carbon) | 10 | 10/24 O (oxygen) | 2 | 2/24 H (hydrogen) | 10 | 10/24 Check: 2/24 + 10/24 + 2/24 + 10/24 = 1 Compute atom percents using the atom fractions: | number of atoms | atom percent Br (bromine) | 2 | 2/24 × 100% = 8.33% C (carbon) | 10 | 10/24 × 100% = 41.7% O (oxygen) | 2 | 2/24 × 100% = 8.33% H (hydrogen) | 10 | 10/24 × 100% = 41.7% Look up the atomic mass, m_i, in unified atomic mass units, u, for each element in the periodic table: | number of atoms | atom percent | atomic mass/u Br (bromine) | 2 | 8.33% | 79.904 C (carbon) | 10 | 41.7% | 12.011 O (oxygen) | 2 | 8.33% | 15.999 H (hydrogen) | 10 | 41.7% | 1.008 Multiply N_i by m_i to compute the mass for each element. Then sum those values to compute the molecular mass, m: | number of atoms | atom percent | atomic mass/u | mass/u Br (bromine) | 2 | 8.33% | 79.904 | 2 × 79.904 = 159.808 C (carbon) | 10 | 41.7% | 12.011 | 10 × 12.011 = 120.110 O (oxygen) | 2 | 8.33% | 15.999 | 2 × 15.999 = 31.998 H (hydrogen) | 10 | 41.7% | 1.008 | 10 × 1.008 = 10.080 m = 159.808 u + 120.110 u + 31.998 u + 10.080 u = 321.996 u Divide the mass for each element by m to calculate mass fractions. Then use the property that mass fractions must sum to one to check the work: | number of atoms | atom percent | mass fraction Br (bromine) | 2 | 8.33% | 159.808/321.996 C (carbon) | 10 | 41.7% | 120.110/321.996 O (oxygen) | 2 | 8.33% | 31.998/321.996 H (hydrogen) | 10 | 41.7% | 10.080/321.996 Check: 159.808/321.996 + 120.110/321.996 + 31.998/321.996 + 10.080/321.996 = 1 Compute mass percents using the mass fractions: Answer: | | | number of atoms | atom percent | mass percent Br (bromine) | 2 | 8.33% | 159.808/321.996 × 100% = 49.63% C (carbon) | 10 | 41.7% | 120.110/321.996 × 100% = 37.30% O (oxygen) | 2 | 8.33% | 31.998/321.996 × 100% = 9.937% H (hydrogen) | 10 | 41.7% | 10.080/321.996 × 100% = 3.130%
Elemental oxidation states
The first step in finding the oxidation states (or oxidation numbers) in 2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone is to draw the structure diagram. Next set every oxidation number equal to the atom's formal charge: In 2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone hydrogen is not bonded to a metal with lower electronegativity, so it will have an oxidation state of +1. Any element bonded to hydrogen gains the bonding electrons, decreasing their oxidation state by 1 for every bond: With hydrogen out of the way, look at the remaining bonds. There are 2 bromine-carbon bonds, 2 carbon-oxygen bonds, and 10 carbon-carbon bonds. For each of these bonds, assign the bonding electrons to the most electronegative element. First examine the bromine-carbon bonds: element | electronegativity (Pauling scale) | Br | 2.96 | C | 2.55 | | | Since bromine is more electronegative than carbon, the electrons in these bonds will go to bromine. Decrease the oxidation number for bromine in every highlighted bond (by 1 for single bonds, 2 for double bonds, and 3 for triple bonds), and increase the oxidation number for carbon accordingly: Next look at the carbon-oxygen bonds: element | electronegativity (Pauling scale) | C | 2.55 | O | 3.44 | | | Since oxygen is more electronegative than carbon, the electrons in these bonds will go to oxygen: Next look at the carbon-carbon bonds: element | electronegativity (Pauling scale) | C | 2.55 | C | 2.55 | | | Since these elements are the same the bonding electrons are shared equally, and there is no change to the oxidation states: Now summarize the results: Answer: | | oxidation state | element | count -3 | C (carbon) | 3 -2 | O (oxygen) | 2 -1 | Br (bromine) | 2 | C (carbon) | 1 0 | C (carbon) | 2 +1 | C (carbon) | 2 | H (hydrogen) | 10 +2 | C (carbon) | 2
Orbital hybridization
First draw the structure diagram for 2, 5-dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone, and for every non-hydrogen atom, count the σ-bonds. Note that double and triple bonds consist of one σ-bond together with one or two π-bonds: Identify those atoms with lone pairs: Find the steric number by adding the lone pair count to the number of σ-bonds: Consult the following chart to determine the hybridization from the steric number: steric number | hybridization 2 | sp 3 | sp^2 4 | sp^3 5 | dsp^3 6 | d^2sp^3 7 | d^3sp^3 Now assign the hybridization for each atom: Answer: | |
Topological indices
vertex count | 24 edge count | 24 Schultz index | 4200 Wiener index | 1107 Hosoya index | 18360 Balaban index | 3.493