It is in an incorrect spot i think
Answer:
See explanation
Explanation:
All molecules possess the London dispersion forces. However London dispersion forces is the only kind of intermolecular interaction that exists in nonpolar substances.
So, the only kind of intermolecular interaction that exists in dimethyl ether is London dispersion forces.
As for ethyl alcohol, the molecule is polar due to the presence of polar O-H bond. In addition to London dispersion forces, dipole-dipole interactions and specifically hydrogen bonding also occurs between the molecules.
Because ethyl alcohol is polar, it is more soluble in water than dimethyl ether.
Answer: C
Explanation:
According to Neils Bohr, atoms contain electrons which are arranged in energy levels. The energy levels proceed from the lowest to the highest. When energy is supplied to an atom,it moves from lower to higher energy levels. The higher energy level is known as the excited state. Excited states are short lived and atoms quickly return to ground state with emission of the absorbed energy in the form of visible light. This visible light must have one of the seven colours observed in the visible spectrum; Red, orange, yellow, indigo, blue, green, violet. Energy required for this excitation is supplied by heating the substance in a flame.
Answer:
ane, al, keto
ol, al, keto
ol, al, one
ol, ane, one.
Explanation:
The suffix –ol is used in organic chemistry principally to form names of organic compounds containing the hydroxyl (–OH) group, mainly alcohols (also phenol). The suffix was extracted from the word alcohol. The suffix also appears in some trivial names with reference to oils (from Latin oleum, oil).
Functional group is a ketone, therefore suffix = -one
Hydrocarbon structure is an alkane therefore -ane
The longest continuous chain is C5 therefore root = pent
The first point of difference rule requires numbering from the left as drawn to make the ketone group locant 2-
pentan-2-one or 2-pentanone
CH3CH2CH2C(=O)CH3
