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The reaction between ethene and HCl results in the addition of the hydrogen chloride across the carbon-carbon double bond in ethene. This leads to the formation of chloroethane (C2H5Cl) as the product.

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Ethene reacts with water to form ethanol This type of raction is called?

Such reactions are known as HYDRATION and are performed in presence of sulphuric acid.


What forms when Ethene combines with sulfur monochloride?

When ethene combines with sulfur monochloride, the reaction forms vinyl sulfide. This is an addition reaction where the double bond in ethene reacts with the sulfur monochloride to form a new carbon-sulfur bond in the product.


Is HCl(aq) C2H4(aq)C2H5Cl(aq) considered a reaction mechanism?

No. This is a reaction, but not a reaction mechanism. The mechanism would should the individual steps or alterations that take place with the HCl dissociating, and the electrons moving from one place to another, etc.


If ethene reacts with chlorine the only product is CH2 Cl-CH2Cl What type of reaction took place?

This is an addition reaction, as the double carbon-carbon bond in ethene breaks to accomodate the two chlorine atoms. Product is 1,2, dichloroethane


Does ethene change from orange to colourless when it reacts with bromine water?

Yes, ethene reacts with bromine water to form a colourless solution. In the presence of ethene, the orange-brown color of bromine water disappears as bromine is consumed in the addition reaction with ethene to form a colourless compound.


Why is the reaction of ethene with bromine called an addition reaction?

Br2 + C2H4 → C2H4Br2 ORBr2 + CH2=CH2 → BrCH2CH2BrThe name of the reaction is pretty intuitive. Ethene's double bond is broken which leaves room for bromine to be added to form dibromoethane.


What is the reaction of ethene with bromine in aqueous solution of sodium chloride?

When ethene reacts with bromine in an aqueous solution of sodium chloride, the bromine adds across the carbon-carbon double bond in ethene through electrophilic addition. This reaction forms a dibromoethane product. The presence of sodium chloride in the aqueous solution helps to generate hypobromous acid, which is the active bromine species that reacts with ethene. This reaction is an example of halogenation of alkenes.


Does ethene react with Bromine in the presence of UV light?

Yes, however it doesn't require it either to react. ethene+bromine water→1,2-dibromoethane Ethane reacts with bromine only in the presence of UV forming bromoethane and hydrogen bromide.


Why the reaction of ethene with bromine called an addition reaction?

Br2 + C2H4 → C2H4Br2 ORBr2 + CH2=CH2 → BrCH2CH2BrThe name of the reaction is pretty intuitive. Ethene's double bond is broken which leaves room for bromine to be added to form dibromoethane.


Can ethene and bromine react without sunlight?

Yes, ethene and bromine can react without sunlight. The reaction occurs through an electrophilic addition mechanism, where bromine adds across the double bond of ethene to form 1,2-dibromoethane. This reaction can proceed in the dark, typically in a non-polar solvent, and is driven by the reactivity of the bromine molecule with the double bond of ethene.


Why is the reason of ethene with bromine called an addition reaction?

The reaction of ethene with bromine is called an addition reaction because the bromine atoms add across the double bond of ethene to form a single product molecule. The double bond in ethene breaks and new single bonds are formed with bromine, resulting in an overall increase in the number of atoms in the product compared to the reactants. This type of reaction is characteristic of addition reactions where atoms or groups are added to a double or triple bond.


What type of chemical reaction is involved in the synthesis of the polymer polyethylene from ethene monomers?

The synthesis of polyethylene from ethene monomers involves a polymerization reaction, specifically addition polymerization. In this process, ethene (an alkene) undergoes a reaction where the double bonds between carbon atoms are broken, allowing the monomers to link together and form long chains of polyethylene. This reaction typically requires catalysts and can occur under heat and pressure.