Answer:
See attached picture.
Explanation:
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In this case, since C2H3Cl is an organic compound we need a central C-C parent chain to which the three hydrogen atoms and one chlorine atom provides the electrons to get all the octets except for H as given on the statement.
In such a way, on the attached picture you can find the required Lewis dot structure without formal charges and with all the unshared electron pairs, considering there is a double bond binding the central carbon atoms in order to compete their octets.
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Because they are coming from the ground and always safe
CH4 + 2O2 =======> CO2 + 2H2O
Answer:
A one-step mechanism involving a transition state that has a carbon partially bonded to both chlorine and oxygen
Explanation:
The compound CH3Cl is methyl chloride. This is a nucleophilic substitution reaction that proceeds by an SN2 mechanism. The SN2 mechanism is a concerted reaction mechanism. This means that the departure of the leaving group is assisted by the incoming nucleophile. The both species are partially bonded to opposite sides of the carbon atom in the transition state.
Recall that an SN2 reaction is driven by the attraction between the negative charge of the nucleophile (OH^-) and the positive charge of the electrophile (the partial positive charge on the carbon atom bearing the chlorine leaving group).