Answer:
See explanation and image attached
Explanation:
Aromatic compounds undergo electrophilic aromatic substitution reactions in which the aromatic ring is maintained.
Substituted benzenes may be more or less reactive towards electrophilic aromatic substitution than benzene depending on the nature of the substituent present in the ring.
Substituents that activate the ring towards electrophilic substitution such as -OCH3 are ortho-para directing.
The major products of the bromination of anisole are p-bromoanisole and o-bromoanisole. The resonance structures leading to these products are shown in the image attached.
Answer:
Option D. Saturated alkane
Explanation:
To know which option is correct, it is important that we know what saturated and unsaturated compounds are in this context.
Saturated hydrocarbons are compounds which has only carbon to carbon single bonds (C–C) in its chain. A very good example of such compound is the Alkanes.
Unsaturated hydrocarbons are compounds which has either a carbon to carbon double bond (C=C) or a carbon to carbon triple bond (C≡C) in its chain. Examples of such compounds include alkenes and alkynes.
Now, let us answer the question given above bearing the meaning of saturated and unsaturated compounds in mind.
The compound given above contains only carbon to carbon (C–C) single bond.
Therefore, the compound is a saturated alkane.
Make sure that you understand what they are asking you from this question, as it can be confusing, but the solution is quite simple. They are stating that they want you to calculate the final concentration of 6.0M HCl once a dilution has been made from 2.0 mL to 500.0 mL. They have given us three values, the initial concentration, initial volume and the final volume. So, we are able to employ the following equation:
C1V1 = C2V2
(6.0M)(2.0mL) = C2(500.0mL)
Therefore, the final concentration, C2 = 0.024M.
Answer:
Two possible compounds are shown below- one with an exocyclic double bond and another one with an endocyclic double bond
Explanation:
Reaction of alkene with 
gives a complex of mercurous ion.
Then water molecule attacks this complex through 
type reaction at more substituted position.
cleaves the resultant C-Hg bond and forms a C-H bond.
Two possible structures of an alkene is possible to yield 1-methylcyclohexanol which are shown below.
The answer is False. Absorption is the process or action by which one thing absorbs or is absorbed by another.
