<span><span>Argon,</span><span>Carbon dioxide,</span><span>Neon,</span><span>Helium, and </span><span>Methane</span></span>
I believe that the choices for this question are:
C2H4O2, C4H8O4 CH2O, C6H12O6 C3H6O3, C6H12O6 C2H4O2, C6H12O6
The answer to this based on the molar masses given is:
C2H4O2, C6H12O6
To prove calculate the molar mass:
C2H4O2 = 2*12 + 4*1 + 2*16 = 60
C6H12O6 = 6*12 + 12*1 + 6*16 = 180
The molecular structure of 1-nitrobutane is . The structure of 1-nitrobutane is shown below.
An atom's formal charge would be determined by the covalent model of chemical bonding, which assumes that almost all chemical bonds include equal sharing of electrons among all atoms, regardless their relative electronegativity.
The structure for 1-nitrobutane, making sure to add all non-zero formal charges
There are four kind of molecule present in 1-nitrobutane and they are carbon, hydrogen , nitrogen and oxygen. Nitrogen is bonded with two oxygen atom out of them one oxygen atom is attached with single bond and second oxygen atom is bonded with double bond. Nitrogen has positive charge whereas oxygen has negative charge.
It is a kind of alkane in with nitro group is attached with alkane group.
To know more about 1-nitrobutane
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The proton which is easily abstracted in
1-Benzyl-3-propylbenzene is the proton which is present on carbon atom in between two phenyl rings, or the central carbon which is shared by two benzene rings.
This easy abstraction of proton is due to its high acidity. Remember those species are always more acidic whose
conjugate base is stable. Like the acidity of carboxylic acid is due to stability of the
acetate ion.
In our case the stability of conjugate base arises due to
stability of negative ion due to resonance. As shown below, the negative charge can delocalize on both rings.
I have shown the resonance of negative ion on both Phenyl rings with
Blue and
Pink colors.<span />