Lindlar's catalyst Pd/CaCO3 + (CH3COO)2 Pb + quinolene
Hydrocarbons
NOTE : Among isomeric alkanes, the straight chain isomer has higher boiling point than the branched chain isomer.
The greater the branching of the chain, the lower is the boiling point.
Further due to the presence of electrons, these molecules are slightly polar and hence have higher boiling points than the corresponding alkanes.
Thus
follows the order alkynes
alkene
alkanes (straight chain) > branched chain alkanes.
-dichloro butane will exhibit optical isomerism due to the presence of two asymmetric carbon atom.
Completing the sequence of given reactions, Thus
is
Hence
is correct answer.
Alkenes combine with hydrogen under pressure and in presence of a catalyst
or
and form alkanes.
Both Statement I and Statement II are correct.
Anti addition of hydrogen atoms to the the triple bond occurs when alkynes are reduced with sodium (or lithium) metal in ammonia, ethylamine, or alcohol at low temperatures.
This reaction called, a dissolving metal reduction, produces an
- or
-alkene. Sodium in liq.
is used as a source of electrons in the reduction of an alkyne to a
alkene.
Polysubstitution is a major drawback of Friedal–Craft alkylation. –CH3 group in highly activating group due to +H effect, so after first time addition of -CH3 group in benzene ring the reactivity of the benzene ring increases.
We know, conbustion of Hydrocarbon Cx Hy + (x +
)O2 x CO2 +
H2O So, to consume 1 mole of Cx Hy we need (x +
) mole of O2 gas.
As both Cx Hy and O2 are gas, So avogadro's law is applicable on them.
At constant temperature and pressure according to avogadro's law, volume mole So, for 5L of Cx Hy the volume of O2 = 5(x +
) According to the question, 5(x +
) = 25
(x +
) = 5 . . . . . (1) For Ethane (C2 H6), x = 2 and y = 6
x +
= 2 +
5
C2 H6 can't be the required alkane. For Propane (C3 H8), x = 3. and y = 8
x +
= 3 +
= 5
Propane (C3 H8) is the right alkane. Similarly for Butane (C4 H10) and Isobutane (C4 H10) you can check x +
5.
Among CH CH and CH2 = CH2, in CH CH compound H atom is attached with sp hybridised C atom and in CH2 = CH2 compound H atom is attached with sp2 hybridised C atom.
As we know, electronegitivity of sp carbon is more compare to sp2 carbon atom and that H is more acidic which is attached with more electronegative carbon atom.
So CH CH is more acidic than CH2 = CH2.
Among CH CH and CH3–C CH, in CH CH both the H atom is connected to sp carbon atom but in CH3–C CH, with one sp carbon atom H atom attached and with other sp carbon atom -CH3 group attached which have +I effect and we know +I effect decreases acidic strength.
So, CH CH is more acidic than CH3–C CH.
So correct order is HC CH > CH3 – C CH > CH2 = CH2