Solve
Guides
0
You visited us 0 times! Enjoying our articles? Unlock Full Access!
Question

In the study of chlorination of propane , four products A , B , C and D of the formula $$ C_3H_6Cl_2 $$ were isolated . Each of them was further chlorinated to provide trichloro products , $$ C_3H_5Cl_3 $$ . It was found that A provided one trichloro product , B gave two and C and D each gave three . What are the structural formulae of A , B , C and D ?

Open in App
Solution
Verified by Toppr


Was this answer helpful?
2
Similar Questions
Q1
During the dichlorination of propane, four products are obtained A,B,C and D with the formula C3H6Cl2 and were isolated. Each of them were further chlorinated to give trichloro products, C3H5Cl3. If A gave only one trichloro product, B gave two and both C & D gave three, which of the following is/are true?
View Solution
Q2
On chlorination of propane, the number of products of the formula C3H6Cl2 is ( only structural isomers ) :
View Solution
Q3
A white precipitate was formed slowly when silver nitrate was added to a compound $$(A)$$ with molecular formula $$C_6H_{13}Cl$$. Compound $$(A)$$ on treatment with hot alcoholic $$KOH$$ gave a mixture of two isomeric alkenes $$(B)$$ and $$(C)$$, having formula $$C_6H_{12}$$. The mixture of $$(B)$$ and $$(C)$$, on ozonolysis furnished four compounds.
a. $$CH_3CHO$$
b. $$C_2H_5CHO$$
c. $$CH_3COCH_3$$
d. $$(CH_3)_2CHCHO$$
What are the structures of $$(A), (B)$$ and $$(C)$$?
View Solution
Q4

Two students were performing some experiments in an organic chemistry laboratory. An unknown compound A, which was found to be a hydrocarbon was subjected to the following reactions. A reaction with chlorine in the presence of light gave compound B, which was divided into two parts. To the 1st part aqueous KOH was added and to the second part, alcoholic KOH was added, product C and D were formed, respectively. C was subjected to oxidation to give another compound. The compound formed was the same as the compound formed by the ozonolysis product of the position isomer of 1-Butene. Identify A, B, C, and D.


View Solution
Q5
A compound ′A′ formula of C3H6Cl2 on reaction with alkali can give ′B′ of formula C3H6O or ′C′ of formula C3H4.′B′ on oxidation gave a compound of the formula C3H6O2.′C′ with dilute H2SO4 containing Hg2+ ion gave ′D′ of formula C3H6O, which with bromine and alkali gave the sodium salt of C2H4O2. Then ′A′ is :
View Solution