Iron exhibits bcc structure at room temperature. Above 900°C, it transforms to fcc structure. The ratio of density of iron at room temperature to that at 900°C (assuming molar mass and atomic radii of iron remains constant with temperature) is
1/2
Consider the following species:
CN+, CN–, NO and CN
Which one of these will have the highest bond order?
NO
CN-
CN
CN+
The correct order of N-compounds in its decreasing order of oxidation states is
HNO3, NH4Cl, NO, N2
HNO3, NO,NH4Cl, N2
HNO3, NO, N2, NH4Cl
NH4Cl, N2, NO, HNO3
Which of the following compounds can form a zwitter ion?
Aniline
Acetanilide
Glycine
Benzoic acid
Regarding cross-linked or network polymers, which of the following statements is incorrect?
They contain covalent bonds between various linear polymer chains.
They are formed from bi- and tri-functional monomers.
They contain strong covalent bonds in their polymer chains.
Examples are bakelite and melamine.
Nitration of aniline in strong acidic medium also gives m-nitroaniline because
Inspite of substituents nitro group always goes to only m-position.
In electrophilic substitution reactions amino group is meta directive.
In acidic (strong) medium aniline is present as anilinium ion.
In absence of substituents nitro group always goes to m-position.
C.
In acidic (strong) medium aniline is present as anilinium ion.
In acidic medium, aniline is protonated to form anilinium ion which is meta-directing.
Hence besides para (51%) and ortho (2%), meta product (47%) is also formed in significant yield.
The difference between amylose and amylopectin is
Amylopectin have 1 → 4 α-linkage and 1 → 6 α-linkage
Amylose have 1 → 4 α-linkage and 1 → 6 β-linkage
Amylose is made up of glucose and galactose
Amylopectin have 1 → 4 α-linkage and 1 → 6 β-linkage
The compound A on treatment with Na gives B, and with PCl5 gives C. B and C react together to give diethyl ether. A, B and C are in the order
C2H5OH, C2H6, C2H5Cl
C2H5OH, C2H5Cl, C2H5ONa
C2H5OH, C2H5ONa, C2H5Cl
C2H5Cl, C2H6, C2H5OH
The compound C7H8 undergoes the following reactions:
The product 'C' is
m-bromotoluene
o-bromotoluene
p-bromotoluene
3-bromo-2,4,6-trichlorotoluene