Maths-
General
Easy
Question
A gas in an open container is heated from 27°C to 127°C. The fraction of the original amount of gas remaining in the container will b
Hint:
A gas is heated in open container. It is heated between two temperatures. We have to find the original fraction of gas left behind when it's heated. We will use the ideal gas equation and find the constant and variable values.
The correct answer is: 
The ideal gas equation is PV = nRT
As the gas is heated in an open container, it's pressure is constant. The volume of the container is constant too. R is a constant.
n is number of moles and T is temperature. n denotes the amount of gas.
So, the above equation is nT = constant.
So, the temperature is inversely proportional to the gas.
The temperature they are heated from his 27°C to 127°C.
Let n1 be the original amount of gas and T1 be temperature at that time.
Let n2 be the amount of gas left after its heated. T2 is the temperature at that time.
We will write the temperature in Kelvin.
T1 = 27 + 273 = 300K
T2 = 127 + 273 = 400k
We know that nT= constant
So, we can write
n2T2 = n1T1
Dividing both the sides by T2

It means
fraction of orginal amount is left.
For such questions, we should know idea gas equation. We have to be careful about constant and variable values. And we always have to convert the temperature into Kelvin. To convert the temperature in °C into Kelvin, we add 273 to it.
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The removal of two atoms or groups, one generally hydrogen
and the other a leaving group
resulting in the formation of unsaturated compound is known as elimination reaction.

In
(elimination) reactions, the
bond is broken heterolytic ally (in step 1) to form a carbocation (as in
reaction) in which
) is lost (rate determining step). The carbocation (in step 2) loses a proton from the
-carbon atom by a base (nucleophile) to form an alkene.
reaction is favoured in compounds in which the leaving group is at secondary
or tertiary
position. In
formed simultaneously.
reactions occur in one step through a transition state.

reactions are most common in haloalkanes (particularly,
) and better the leaving group higher is the
reaction. In
reactions, both the leaving groups should be antiplanar.
cb (Elimination unimolecular conjugate base) reaction involves the removal of proton by. a conjugate base (step 1) to produce carbanion which loses a leaving group to form an alkene (step 2) and is a slow step.
2-Bromobutane on heating with concentrated solution of alcoholic KOH gives major product as:
The removal of two atoms or groups, one generally hydrogen
and the other a leaving group
resulting in the formation of unsaturated compound is known as elimination reaction.

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(elimination) reactions, the
bond is broken heterolytic ally (in step 1) to form a carbocation (as in
reaction) in which
) is lost (rate determining step). The carbocation (in step 2) loses a proton from the
-carbon atom by a base (nucleophile) to form an alkene.
reaction is favoured in compounds in which the leaving group is at secondary
or tertiary
position. In
formed simultaneously.
reactions occur in one step through a transition state.

reactions are most common in haloalkanes (particularly,
) and better the leaving group higher is the
reaction. In
reactions, both the leaving groups should be antiplanar.
cb (Elimination unimolecular conjugate base) reaction involves the removal of proton by. a conjugate base (step 1) to produce carbanion which loses a leaving group to form an alkene (step 2) and is a slow step.
2-Bromobutane on heating with concentrated solution of alcoholic KOH gives major product as:
Chemistry-General
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The removal of two atoms or groups, one generally hydrogen
and the other a leaving group
resulting in the formation of unsaturated compound is known as elimination reaction.

In
(elimination) reactions, the
bond is broken heterolytic ally (in step 1) to form a carbocation (as in
reaction) in which
) is lost (rate determining step). The carbocation (in step 2) loses a proton from the
-carbon atom by a base (nucleophile) to form an alkene.
reaction is favoured in compounds in which the leaving group is at secondary
or tertiary
position. In
formed simultaneously.
reactions occur in one step through a transition state.

reactions are most common in haloalkanes (particularly,
) and better the leaving group higher is the
reaction. In
reactions, both the leaving groups should be antiplanar.
cb (Elimination unimolecular conjugate base) reaction involves the removal of proton by. a conjugate base (step 1) to produce carbanion which loses a leaving group to form an alkene (step 2) and is a slow step.
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and the other a leaving group
resulting in the formation of unsaturated compound is known as elimination reaction.

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(elimination) reactions, the
bond is broken heterolytic ally (in step 1) to form a carbocation (as in
reaction) in which
) is lost (rate determining step). The carbocation (in step 2) loses a proton from the
-carbon atom by a base (nucleophile) to form an alkene.
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position. In
formed simultaneously.
reactions occur in one step through a transition state.

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reaction. In
reactions, both the leaving groups should be antiplanar.
cb (Elimination unimolecular conjugate base) reaction involves the removal of proton by. a conjugate base (step 1) to produce carbanion which loses a leaving group to form an alkene (step 2) and is a slow step.
Isopropyl chloride on heating with concentrated solution of ethanolic KOH gives mainly:
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