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What is the mechanism for the reaction between bromine and cyclohexane and state the conditions favor the reaction?
Wiki User
∙ 11y ago
electrophilic substitution. and UV light or heat is required to all the reaction to proceed
Wiki User
∙ 11y ago
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What is the reaction between acrylic acid and titanium dioxide?
what is the reaction mechanism between acrylic acid,4-vinyl pyridine
What Difference between reactivity in hexane and cyclohexane?
Not much. Both are alkanes, and alkanes are highly unreactive. The only reaction for alkanes I can think of off the top of my head is free radical halogenation, but both hexane and cyclohexane have secondary carbons, so reactivity is comparable. Of course, cyclohexane has 6 secondary carbons while hexane only has 4, so you can make the argument that cyclohexane is more reactive in this example.
Mechanism for the formation of the semicarbazone derivative?
Click the related link below to see the mechanism for the condensation reaction between semicarbazide and a carbonyl compound to form semicarbazone.
What is difference between process and mechanism?
process is process and mechanism is mechanism.
What is the product of hexane 2 5 dione and NaOH?
Cyclohexane-1,4-dione. this reaction mechanism follows Baldwin's rule of ring formation, when the hydroxide attacks the alpha carbon on hexane-2,5-dione, it gives the product a double bond on the alpha carbon and puts a negative charge on the oxygen, the electrons from the double bond are then used to create a bond between Carbon-1 and Carbon-6. Giving you a carbonyl group on each end of the ring. It helps when you're writing out the mechanism to draw the hexane-2,5-dione in the formation of an aromatic ring!
What is the equation for the reaction between cyclohexane and sodium hydroxide?
There is no reaction, therefore no equation!!
What is the product of cyclohexane and toluene?
there is no chemical reaction between these two.
What is the mechanism of reaction between Wagner's reagent and alkaloids?
what is the reaction mechanism between wagner's reagent and alkaloids
What the reaction mechanism between the m-phenylenediamine and trimesoylchloride?
The reaction mechanism between these two chemicals involved an aromatic carbon. The typical classification of this reaction is called a condensation.
What is the reaction between acrylic acid and titanium dioxide?
what is the reaction mechanism between acrylic acid,4-vinyl pyridine
What Difference between reactivity in hexane and cyclohexane?
Not much. Both are alkanes, and alkanes are highly unreactive. The only reaction for alkanes I can think of off the top of my head is free radical halogenation, but both hexane and cyclohexane have secondary carbons, so reactivity is comparable. Of course, cyclohexane has 6 secondary carbons while hexane only has 4, so you can make the argument that cyclohexane is more reactive in this example.
Mechanism for the formation of the semicarbazone derivative?
Click the related link below to see the mechanism for the condensation reaction between semicarbazide and a carbonyl compound to form semicarbazone.
What is the product of the reaction between cyclohexane and acidified potassium manganate VII?
The product of the reaction between cyclohexene and hot acidified potassium manganate 7 will be cyclohexan-1,2-diol. Two hydroxy groups will bond at the site of the double bond.
What is difference between process and mechanism?
process is process and mechanism is mechanism.
What is the product of hexane 2 5 dione and NaOH?
Cyclohexane-1,4-dione. this reaction mechanism follows Baldwin's rule of ring formation, when the hydroxide attacks the alpha carbon on hexane-2,5-dione, it gives the product a double bond on the alpha carbon and puts a negative charge on the oxygen, the electrons from the double bond are then used to create a bond between Carbon-1 and Carbon-6. Giving you a carbonyl group on each end of the ring. It helps when you're writing out the mechanism to draw the hexane-2,5-dione in the formation of an aromatic ring!
What is conditions of reaction between phthalic anhydride and resorcinol?
Zinc chloride and an acid must be present, preferably HCl
Why is there an extraordinary difference in melting points between cyclohexane and cyclohexene?
The extraordinary difference in melting points between cyclohexane and cyclohexene is due to the difference in shape. Cyclohexene has an awkward geometry to stack with sp2 hybridized bond angles. This lends to an extreme low melting point for cyclohexene.
