This is because the longer the carbon chain, it spreads it out more equally which causes the carbon to get a lot more thicker and less runny
Answered by a natural scientist who tries the experiments
The longer the carbon chain, it spreads out the atoms more equally which causes the carbon to get thicker and less runny.
The general formula for alkadienes is CnH2n-2, where n represents the number of carbon atoms in the alkadiene chain. This formula indicates that alkadienes have two fewer hydrogen atoms than alkanes of the same carbon chain length, due to the presence of two double bonds in their structure.
The heat of combustion for decane is approximately -6,316 kJ/mol. This value represents the amount of heat released when one mole of decane is completely burned in oxygen to form carbon dioxide and water.
A carbon-carbon double bond is longer than a carbon-carbon single bond because the presence of the additional pi bond in the double bond results in more electron-electron repulsions, causing the double bond to be longer in length compared to a single bond.
Carbon. Organic molecules are usually made up of carbon chains or rings, with hydrogen atoms bonded to most bond sites. The molecules are distinguished by the length of the chain, the number of double or triple carbon-carbon bonds, and the other elements or ligands that might be bonded to the carbon chain or ring.
The longer the carbon chain, it spreads out the atoms more equally which causes the carbon to get thicker and less runny.
Viscosity increases with increasing chain length of straight-chain alkanes while that for isomeric alkanes increase with branching because of the difference in the number of rings contained within their hydrocarbons.
When the chain length of carbon increase the flammability decrease.
The C-C bond length in alkanes is typically around 1.54 angstroms, which is a measure of the distance between the carbon atoms in the molecule. This bond length may vary slightly depending on the specific alkane compound and its molecular structure.
the flammability of alkanes decreases as the hydrocarbon chains increase in length their evapouration rates decrease as longer chained molecules have higher boling points so temperatures must be high for them to evaporate therefore there is no fumes or vapours for longer chained alkanes at room temp like nonane and so on these hydrocarbons need higher temp to produce vapours n therefore will not burn with just a match
Boiling points of hydrocarbons generally increase with an increase in the number of carbon atoms. This is because larger hydrocarbons have stronger London dispersion forces due to increased surface area, which requires more energy to overcome during boiling.
A mil is a unit of length equal to 0.001 inches. The more mils, the thicker.
You increase the length of leads of a capacitor by splicing extra length onto them.
Haloalkanes have higher boiling points than alkanes because the electronegative halogen atoms can form dipole-dipole interactions with neighboring molecules, increasing the intermolecular forces. This results in a higher energy requirement to overcome these forces and change the haloalkane from a liquid to a gas.
The heat of combustion for decane is approximately -6,316 kJ/mol. This value represents the amount of heat released when one mole of decane is completely burned in oxygen to form carbon dioxide and water.
absolutely no. length and width are independent parameters .
As the thickness of a convex lens increases, the focal length decreases. This is because a thicker lens has a more curved surface, which causes light to converge more quickly. The focal length is the distance at which the light converges, so a thicker lens leads to a shorter focal length.