Sound waves are longitudinal waves that is, are transmitted in the same direction of oscillation of the particles in the medium. Electromagnetic waves are transverse ie, the electric and magnetic fields, which are perpendicular to each other, oscillate perpendicularly to the direction of wave propagation.
Answer:
cis-1-tert-butyl-3-methylcyclohexane will have a higher percentage of the diequatorial-substituted conformer when compared with the diaxialsubstituted conformer.
Explanation:
The two compound contain or have high stability with the substituent group is at equatorial position but the tert-betyl group in cis-1-tert-butyl-3-methylcyclohexane is larger than the methyl group in trans-1,4-dimethylcyclohexane.
Thus, the equatorial position will be more favorable for the substituent group in the cis-1-tert-butyl-3-methylcyclohexane, therefore having higher percentage of the diequatorial substituted conformer compared with that of diaxial-substituted conformer.
- The answer is shorter wavelength and equal speed.
That is, compared to ultraviolet light, an electromagnetic wave that has a higher frequency will also have shorter wavelength and equal speed.
This can be seen by the reaction given below:
h= Planck's constant
c=speed of the light
=frquency
=wavelength
So, higher is the frequency, lesser is the volume while speed remains constant as c is speed of light.
6 sodium and 6 Bromine in 6NaBr
