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What else can I help you with?
Which one is more polar o-xylene or p-xylene?
Neither!
At what temperature does mixture of water and xylene boil?
Such a mixture would not have a specific boiling point. Instead, it can be used for separating the two substances by heating, a process known as distillation. At 100C, water will begin to evaporate and it can be collected. Only at 138C, will xylene begin to boil and become a gas, ready for collection. Thus, there is no specific melting points for such a mixture. If two liquids are insoluble in each other (as is the case for xylene in water, each phase exerts its own vapor pressure at a given temperature. The total pressure is then the sum of the vapor pressures for each liquid at that temperature. At 94.5 Deg. C the vapor pressures of xylene and water phases total one atmosphere -some 45 Deg. C, cooler than for xylene alone!
Is concentrated Ethanol blue in color?
Ethanol can reach up to 99% purity, which means highest concentration. Pure Ethanol is colorless exactly like water! Any color in ethanol is because of bad distillation or additives!
What are the liquids used in spirit level?
Basically its alcohol and especially ethanol.
What is the reaction of buna rubber?
buna can be synthesised from ethanol 2C2H5OH------> CH2=CH-CH-CH2 +H2O+H2 in the presence of Al203 and ZnO
Full-form of D.P.X mountant?
Dibutyl Phathalate Xylene
Which type of isomers are o-xylene m-xylene and p-xylene?
o-xylene, m-xylene, and p-xylene are positional isomers, meaning they have the same molecular formula but differ in the position of the substituent groups on the benzene ring.
What is a dilute form for ethanol?
A dilute form of ethanol is a solution of ethanol in water. It is commonly referred to as alcohol or ethyl alcohol and is commonly used in various applications such as disinfectants, cleaning solutions, and beverages. The concentration of ethanol in a dilute form can vary, with common percentages like 70% or 90% ethanol.
Is xylene an element or compound?
Xylene is a compound. It is a mixture of three isomeric aromatic hydrocarbons: o-xylene, m-xylene, and p-xylene.
How many types of xylene are?
There are three main types of xylene: ortho-xylene (o-xylene), meta-xylene (m-xylene), and para-xylene (p-xylene). These are isomers of each other, meaning they have the same chemical formula but their atoms are arranged in different ways.
What is the formula of xylene?
Basic equation for xylene is C8H10.Xylene is di-methyl benzene and comes in three different forms (isomers) :1,2-dimethylbenzene also called orthoxylene sometime shortened to o-xylene1,3-dimethylbenzene also called metaxylene sometimes shortened to m-xyleneand1,4-dimethylbenzene also called paraxylene sometimes shortened to p-xylene
Which one is more polar o-xylene or p-xylene?
Neither!
What happens when ethanol reacts with bromine water?
When ethanol reacts with bromine water, the bromine is displaced by the oxygen in ethanol, resulting in decolorization of the bromine water. This reaction occurs because ethanol is a reducing agent, which means it can donate electrons to the bromine atoms, converting them from a colored form (brown/red) to a colorless form.
What is a product made from xylene?
Xylene is generally used as a solvent. It is often encountered as a mixture of three different isomers, (same composition different structure), which are generically dimethylbenzenes.Para-xylene (1, 4 dimethyl benzene) can be oxidised toterephthalicacid which is then used for manufacture of PET plastiic.Xylenes can be chlorinated to form disinfectants (PCMX).
How do you separate ethanol from aqueous ethanol?
Ethanol can be separated from aqueous ethanol through a process called distillation. In distillation, the mixture is heated to evaporate the ethanol, which is then condensed back into liquid form. The condensed ethanol can then be collected as a separate product.
Will xylene melt plastic?
Yes, xylene can melt certain types of plastic.
Which isomer of xylene does form only one trisubstituted benzene?
1,3-dimethylbenzene (meta-xylene) forms only one trisubstituted benzene due to its symmetrical structure, where the two methyl groups are in the meta positions with respect to each other on the benzene ring. This symmetry allows for only one possible trisubstituted product to form.
