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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)

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13y ago

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What could you distinguish octanol from 1-octene by a simple chemical test?

Refer to functional groups. Anything with the suffix -ol will be an alcohol, a OH. Anything ending with the suffix -ene will have an alkene, a C-C double bond. Therefore 1-octanol has an alcohol and 1-octene has a C-C double bond.


What is the product when 2-octene reacts with sulfuric acid?

Assuming there is water present, I would expect the product to be a (roughly equal) mixture of 2-octanol and 3-octanol.


How do you distinguish toluene from 1-octene?

Bromine in CCl4 is instantly decolorized by 1-octene, because it adds to the double bond, giving 1,2-dibromooctane. Toluene does not give this test because it is aromatic and thus does not add halogens.


How many moles of H2 gas should be taken up by 1-octene when 1-octene is changed to n-octane by catalytic hydrogenation?

You need to know how much 1-octene you are starting with. In my lab it was 120 microliters. Change it to liters by dividing by 1000 to make milliliters (mL). I then multiplied by .72 (the density; g/cm3), divided by 112.22 (molecular weight; g/mol). (0.120 mL Octene) x (.72g/cm3) x (1 cm3/1 mL)x (1 mol /112.22 g) x (1 mole H2/1 mole octene). . :)


Is the boiling point of 1-hexene higher or lower than 1-octene?

The boiling point of 1-hexene is 63 0C.The boiling point of 1-octene is 121 0C.


What is the molar heat of combustion of 1-octanol?

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.


What is the equation for 1-octene and h2so4?

The equation for the reaction of 1-octene with sulfuric acid is as follows: H2CCHCH2CH2CH2CH2CH2CH3 + H2SO4 ----> CH3CCHOSO2OHCH2CH2CH2CH2CH2CH3. This is otherwise known as octyl hydrogensulphate. The major product is markovnikov.


Is octanol soluble in 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.


What pairs of compounds would be most easily separated by thin layer chromatography n-octyl alcohol and 1-octene hexadecane and octadecane?

N-octyl alcohol and 1-octene would be most easily separated by thin layer chromatography due to their differences in polarity. Hexadecane and octadecane, being nonpolar hydrocarbons, may be more challenging to separate as their chemical properties are more similar.


Gases produced when 1-Octanol reacts with SOCl2 and pyridine?

HCl and SO2


Ester formed between 1-octanol and glacial acetic acid?

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.


Is 2-octene solubile in water?

No, 2-octene is not soluble in water because it is a nonpolar compound and water is a polar solvent. Nonpolar compounds like 2-octene are not able to form favorable interactions with water molecules, leading to poor solubility.