Maths-
General
Easy
Question
If the minimum value of the expression 
can be expressed in the form 
where a, b N and are in their lowest term then the value of (a + b) equals
- 243
- 245
- 247
- 347
The correct answer is: 247
where a=4,b=
a+b=247
Related Questions to study
Maths-
Consider the lines represented parametically as
L1 : 
L2 : 
Find equation of the plane P containing the line L2 and parallel to the line L1, is
Consider the lines represented parametically as
L1 :
L2 :
Find equation of the plane P containing the line L2 and parallel to the line L1, is
Maths-General
Maths-
let l ,m,n be the D.Cs of a vector 
and a,b,c are three numbers such that a,b,c are proprotionals to l,m,n i.e, 
are direction rations
be a vector having drs 
the angle between two lines whose DCs are 
is 
A vector 
has length 21 and drs 2,3,6 the dcs of when makes an obtuse angle with x-axis is
let l ,m,n be the D.Cs of a vector and a,b,c are three numbers such that a,b,c are proprotionals to l,m,n i.e, are direction rations
be a vector having drs the angle between two lines whose DCs are is
A vector has length 21 and drs 2,3,6 the dcs of when makes an obtuse angle with x-axis is
Maths-General
Maths-
equals to
equals to
Maths-General
Maths-
If A = 
, then det (adj. (adj. A)) is
If A = , then det (adj. (adj. A)) is
Maths-General
Maths-
Let S be a set containing n elements. Then the total number of binary operations on S is
Let S be a set containing n elements. Then the total number of binary operations on S is
Maths-General
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is equal to
is equal to
Maths-General
Maths-
The sum of 
The sum of
Maths-General
Maths-
If x is nearly equal to 1 such that 
, then the value of l is
If x is nearly equal to 1 such that , then the value of l is
Maths-General
Maths-
Greatest term (numerically) in the expansion of 
if 
and 
is
Greatest term (numerically) in the expansion of if and is
Maths-General
Maths-
Co-efficient of 
in the expansion of 
is
Co-efficient of in the expansion of is
Maths-General
Chemistry-
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.
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:
Chemistry-General
Chemistry-
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.
Isopropyl chloride on heating with concentrated solution of ethanolic KOH gives mainly:
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.
Isopropyl chloride on heating with concentrated solution of ethanolic KOH gives mainly:
Chemistry-General
Chemistry-
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Above compound on treatment with NBS gives allylic bromides. How many product(s) will be obtained in this reaction?
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Above compound on treatment with NBS gives allylic bromides. How many product(s) will be obtained in this reaction?
Chemistry-General
Chemistry-
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Which of the following sequences is correct about C-H bond energy?
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Which of the following sequences is correct about C-H bond energy?
Chemistry-General
Chemistry-
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Consider the three types of C-H bonds in cyclohexene.
Which of the following is/are correctly matched?
Karl Ziegler reported that alkenes react with N-bromosuccinimide (NBS) in presence of light to give products resulting from substitution of hydrogen by bromjne at the allylic position, i.e., the position next to the double bond. Let us consider the halogenation of cyclohexene.
Energy level diagram for allylic, vinylic and alkylic, free radicals is .given below:
Consider the three types of C-H bonds in cyclohexene.
Which of the following is/are correctly matched?
Chemistry-General
