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When 0.515g of biphenyl C12H10 undergoes combustion in a bomb calorimeter the temperature rises from 25.9C to 30.0circ C?
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What is the melting point of biphenyl?
the melting point of biphenyl is 70 degrees Celsius.
Is chlorobenzene polar or non polar?
Biphenyl has equal charges on both benzene rings, this material is non polar
Is Biphenyl aromatic or aliphatic compound?
Biphenyl is a non planar molecule and hence should'nt be aromatic.
Is diphenylmethane solid at room temperature?
The melting point of diphenyl (Biphenyl) is 156.6 degrees Fahrenheit, so it is a solid at room temperature. Acetone has a melting point of -139 degrees Fahrenheit, so it is a liquid at room temperature.
Why is Biphenyl Soluble in Hexane?
Both are non-polar, thus "like disolves like"
Is biphenyl soluble in ethanol?
biphenyl is soluble in ethanol and also in most of organic solvents
What is the chemical formula for biphenyl?
The chemical formula for biphenyl is C12H10
Acetyl chloride plus aluminum chloride with biphenyl?
4-acetyl biphenyl
What is a biphenyl?
A biphenyl is a substituted or otherwise altered version of the hydrocarbon C12H10, such as PCBs.
What is the melting point of biphenyl?
the melting point of biphenyl is 70 degrees Celsius.
Is chlorobenzene polar or non polar?
Biphenyl has equal charges on both benzene rings, this material is non polar
What is an aminobiphenyl?
An aminobiphenyl is an amine derivative of biphenyl.
What is the difference between Biphenyl and naphthalene?
The difference between Biphenyl and naphthalene is that Biphenyl is two phenyl groups linked by a single bond from a carbon on one phenyl group to another. Naphthalene shares two carbon atoms in between two phenyl groups.
Is Biphenyl aromatic or aliphatic compound?
Biphenyl is a non planar molecule and hence should'nt be aromatic.
What has the author Heinze Stangl written?
Heinze Stangl has written: 'Phenylation of biphenyl, o- and m-terphenyl and their mixtures with benzoylperoxide' -- subject(s): Biphenyl compounds, Chemical kinetics
How are naphthalene and biphenyl similar?
Both are bicyclic aromatic solid compounds insoluble in water
How do eliminate biphenyl as a by product in a Grignard reaction?
Biphenyl will be dissolved in ether along with your desired product after Grignard synthesis. If you add an aqueous sodium hydroxide (NaOH) solution to this it will react with your desired product but not the biphenyl and form two layers of solution. One layer will be biphenyl dissovled in ether the other will be NaX (where X is your desired product, just with the Na attached to an oxygen rather than a H) dissolved in water. The latter solution can be separated with a separatory funnel; it will be the lower layer. To precipitate you product from its aqueous solution just cool it and add hydrochloric acid (HCl). There you have it, that's how to eliminate byphenyl from your desired product. Hope it helped.
