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Alkynes undergo many addition reactions such as: catalytic hydrogenation, addition by electrophilic reagents, hydration with tautomerism, hydroboration reactions, and oxidations. They also undergo nucleophilic addition reactions & reduction. Finally alkynes are the strongest bronsted acids made from only hydrocarbons.
the electron in benzene are delocalised making d ring to be elctron rich,thereby undergoing electrophilic substitution.benzene cannot undergo nucleophillic substitution,it can only undergo if it is substituted with an electron withdrawing group
Elements tend to undergo chemical reactions that increase stability.
Pyridine will add to carbon 3 in electrophilic reactions, such as Bromine addition. However in a nucleophilic reaction, such as seen in the Chichibabin reaction, carbon #2 and #4 are substituted such as if NH2 - attacked. Draw out the resonance forms and you will see this, or consult any Organic text under heterocyclic Chemistry.In a C3 attack, the electrophile will destabilize the C2 and C4 position, to a great extent since N lacks an octet in one of these resonance forms.In a nucleophilic addition, addition at C2 or C4 allows the negative charge to be shared by Nitrogen thus is preferred to the C3 attack. Hope that helps. Dr Jim Romano CEO Romano Scientific CEO Orgoman.com Class of 1991 NYU
no they dont
Alkynes undergo many addition reactions such as: catalytic hydrogenation, addition by electrophilic reagents, hydration with tautomerism, hydroboration reactions, and oxidations. They also undergo nucleophilic addition reactions & reduction. Finally alkynes are the strongest bronsted acids made from only hydrocarbons.
Alkanes like (methane, ethane, propane etc.) … They do not undergo addition reactions
the electron in benzene are delocalised making d ring to be elctron rich,thereby undergoing electrophilic substitution.benzene cannot undergo nucleophillic substitution,it can only undergo if it is substituted with an electron withdrawing group
Elements tend to undergo chemical reactions that increase stability.
Do not undergo SN1 reactions.
They undergo similar reactions because they are both in the same group on the periodic table.
Metals undergo neutralization reactions with acids. The products of these reactions are a salt of the metal and the gaseous hydrogen. Direct addition of metal to an acid solution may cause explosions as they are highly exothermic.
Pyridine will add to carbon 3 in electrophilic reactions, such as Bromine addition. However in a nucleophilic reaction, such as seen in the Chichibabin reaction, carbon #2 and #4 are substituted such as if NH2 - attacked. Draw out the resonance forms and you will see this, or consult any Organic text under heterocyclic Chemistry.In a C3 attack, the electrophile will destabilize the C2 and C4 position, to a great extent since N lacks an octet in one of these resonance forms.In a nucleophilic addition, addition at C2 or C4 allows the negative charge to be shared by Nitrogen thus is preferred to the C3 attack. Hope that helps. Dr Jim Romano CEO Romano Scientific CEO Orgoman.com Class of 1991 NYU
no. it is not known to undergo any checmical reactions
no they dont
Alkyl halides undergo both nucleophilic substituions reactions and Elimination reractions depending upon the conditions...In the presence they undergo Elimination Reactions , while in the presence of nucleophile they undergo SN reactions...By: Farman ullah ,Azim kala, masha mansoor, lakki marwat, kpk,Pakistan+92321-9632344
Acids undergo neutralization reactions with bases.