wut the heck is otctene?????????
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). . :)
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.
cis CH3-CH=CHCl trans CH3-CH=CHCl CH3-CCl=CH2 CH2Cl-CH=CH2 Chlorocyclopropane - a cyclopropane with a chlorine attached source http://chemistrysat.blogspot.com/2007/03/sat-question-of-day.html
For example, if you are using Borane tetrahydrofuran, the BH3 that reacts with 1-octene in a hydroboration reaction will violently react with water and cause a reduction of your final product as it is destroyed.
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.
n-octyl alcohol and 1-octene due to the large difference in the polarity between the two.
The boiling point of 1-hexene is 63 0C.The boiling point of 1-octene is 121 0C.
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.
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). . :)
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.
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)
cis CH3-CH=CHCl trans CH3-CH=CHCl CH3-CCl=CH2 CH2Cl-CH=CH2 Chlorocyclopropane - a cyclopropane with a chlorine attached source http://chemistrysat.blogspot.com/2007/03/sat-question-of-day.html
This is a catalyst. You need one drop for this lab. One drop is 50mcL.
Assuming there is water present, I would expect the product to be a (roughly equal) mixture of 2-octanol and 3-octanol.
Polymers are made from monomers and there are many of them. They include olefins such as ethylene, propylene, octene etc and their halogenated analogues. There are many other raw materials that polymers are made from.
There are many of them, starting with octane, octene, and octyne and their numerous possible isomers; octanols and octane diols and triols; ethyl benzene; dimethyl benzene; etc.
For example, if you are using Borane tetrahydrofuran, the BH3 that reacts with 1-octene in a hydroboration reaction will violently react with water and cause a reduction of your final product as it is destroyed.