Answer:c
Explanation:
softwood is used in doors roofs and so on
Answer:
The predominant intermolecular force in the liquid state of each of these compounds:
ammonia (NH3)
methane (CH4)
and nitrogen trifluoride (NF3)
Explanation:
The types of intermolecular forces:
1.Hydrogen bonding: It is a weak electrostatic force of attraction that exists between the hydrogen atom and a highly electronegative atom like N,O,F.
2.Dipole-dipole interactions: They exist between the oppositely charged dipoles in a polar covalent molecule.
3. London dispersion forces exist between all the atoms and molecules.
NH3 ammonia consists of intermolecular H-bonding.
Methane has London dispersion forces.
Because both carbon and hydrogen has almost similar electronegativity values.
NF3 has dipole-dipole interactions due to the electronegativity variations between nitrogen and fluorine.
The enthalpy of reaction for the combustion of ethane 2CH₃CH₃ + 7O₂ → 4CO₂ + 6H₂O calculated from the average bond energies of the compounds is -2860 kJ/mol.
The reaction is:
2CH₃CH₃ + 7O₂ → 4CO₂ + 6H₂O (1)
The enthalpy of reaction (1) is given by:
(2)
Where:
r: is for reactants
p: is for products
The bonds of the compounds of reaction (1) are:
- 2CH₃CH₃: 2 moles of 6 C-H bonds + 2 moles of 1 C-C bond
- 7O₂: 7 moles of 1 O=O bond
- 4CO₂: 4 moles of 2 C=O bonds
- 6H₂O: 6 moles of 2 H-O bonds
Hence, the enthalpy of reaction (1) is (eq 2):

Therefore, the enthalpy of reaction for the combustion of ethane is -2860 kJ/mol.
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The given compound is being synthesized by condensing
Acetone and
Pivaldehyde (Trimethylacetaldehyde).
First Acetone is treated with
Base, the base abstracts the mildly acidic proton present at alpha position to carbonyl group. The resulting specie called
enolate act as a nucleophile and attacks on highly reactive aldehyde which upon
dehydration yields the
Aldol Product. The Reaction is as follow,
Answer:
a, g, c
Explanation:
The conversion of the stable cyclopentane into Trans-1, 2dibromocyclopentane will require three step reactions.
The first is to convert the compound into a cyclopentene, through the addition of Bromine water under heat and photons (light). So option A is the first in the order. This will generate 1 bromocyclopentane through halogenation of the alkane. Secondly, a hot and strong base should be added like the NaOEt, EtOH to remove the added bromine and one atom of hydrogen from the resulting 1 bromocyclopentane in the previous reaction. This will yield cyclopentene, thus making the compound more electrophilic. So option g is required. Thirdly, bromine molecules will be added (C) to take up their places at the two electrophilic regions of the compound to produce Trans-1, 2dibromocyclopentane.