C8H18O that is the formula.
H-c-c-c-c-c-c-c-c-h ( Basic structure before the addition of the other H atoms and the OH)
to each Carbon atom there is two H atoms attached to it on top and on the bottom, therefore each C atom makes 4 bonds. The last carbon on the right will have a OH rather then just a H atom on top. If done properly there should be seven H atoms on the top of the basic structure i gave bonded to the C atoms with the one OH on the last C atom on the right. On the bottom there should be eight H atoms bonded with the C atoms.
The emprical formula of caffeine( C8H10N4O2) is Carbon:Hydrogen:Nitrogen:Oxygen 8 : 10 : 4 : 2 4 : 5 : 2 : 1 So, its empirical formula will be wriiten as C4H5N2O
No, n-octane is nonpolar because it consists of carbon and hydrogen atoms bonded together covalently, resulting in a symmetric distribution of electron density and no permanent dipole moment.
The balanced equation for the complete combustion of octanol is 2C8H18 + 25O2 -> 16CO2 + 18H2O.
The general chemical formula for porphyrins, including heme found in hemoglobin, is C34H32N4O4. Individual porphyrins may have variations in this formula based on their specific structure and substituents.
The formula for aluminate ion is Al(OH)₄⁻ and the valency is -1.
The molar heat of combustion of 1-octanol is approximately -6,268 kJ/mol. This value represents the amount of heat released when one mole of 1-octanol is completely burned in excess oxygen to form carbon dioxide and water.
Octanol is sparingly soluble in water because of its hydrophobic nature. The long hydrophobic carbon chain in octanol is not favorable for interaction with water molecules, preventing it from dissolving easily in water.
1-octanol is an alcohol, so it has an OH group attached to the first C atom. (C8H17OH) 1-octene is an alkene, which has a double bond between the first and second C atoms. (C8H16)
HCl and SO2
The ester formed between 1-octanol and glacial acetic acid is octyl acetate. This reaction involves the condensation of the hydroxyl group of 1-octanol with the carboxyl group of acetic acid, resulting in the formation of the ester bond. Octyl acetate is commonly used as a flavor and fragrance ingredient due to its fruity aroma.
The esterification product between salicylic acid and 1-octanol is octyl salicylate. This compound is commonly used in cosmetics and personal care products as a UV filter due to its UV-absorbing properties.
Thr freezing point of 1-octanol is -16 oC.
Octanol does not have a specific smell as it is a chemical compound. However, some people may describe the smell of octanol as slightly floral, fruity, or waxy. It is important to note that individual perceptions of smell can vary.
Octanol is less dense than water, so it can float on the surface of water. This is because octanol is an organic compound with a lower density than water, allowing it to remain on top when the two liquids are combined.
Yes, hexane is a nonpolar solvent and it can dissolve 1-octanol, which is also a nonpolar substance. This is because like dissolves like, and nonpolar substances tend to dissolve in nonpolar solvents.
Octanol is commonly used as a solvent in chemistry for organic reactions and extractions. It is also used in the pharmaceutical industry for drug formulation and in cosmetics as an emollient. Additionally, octanol is used in research to study membrane permeability and partition coefficient measurements.
Octanol is considered an energy efficient fuel due to its high energy density, which is approximately 30% higher than gasoline. This means that Octanol can provide more energy per unit volume, allowing it to generate more power and efficiency when used as a fuel for engines or vehicles. Additionally, Octanol has a lower risk of evaporation compared to other biofuels, reducing energy losses during storage and transportation.