Its most significant when all other forces are absent
Answer:
See Explanation
Explanation:
According to the question, it is established that the pain caused by a lot of insect bites owes to the acidity of the insect bites.
If this is true, then there is an urgent need to neutralize the acidic insect bite using a basic substance.
Hence the pH of the creams used to treat insect bites should be basic(having a high pH).
2. The compound methene can not exist because it is supposed to be derived from the alkane called methane which contains only one carbon atom.
In order to form an alkene, there must be a double bond between two carbon atoms. This is not possible because there is only one carbon atom in the hypothetical methene. Hence, a compound named methene cannot exist.
<u>Answer:</u> The correct answer is Option D.
<u>Explanation:</u>
To calculate the hybridization of
, we use the equation:
![\text{Number of electron pair}=\frac{1}{2}[V+N-C+A]](https://tex.z-dn.net/?f=%5Ctext%7BNumber%20of%20electron%20pair%7D%3D%5Cfrac%7B1%7D%7B2%7D%5BV%2BN-C%2BA%5D)
where,
V = number of valence electrons present in central atom (S) = 6
N = number of monovalent atoms bonded to central atom = 0
C = charge of cation = 0
A = charge of anion = 0
Putting values in above equation, we get:
![\text{Number of electron pair}=\frac{1}{2}[6]=3](https://tex.z-dn.net/?f=%5Ctext%7BNumber%20of%20electron%20pair%7D%3D%5Cfrac%7B1%7D%7B2%7D%5B6%5D%3D3)
The number of electron pair around the central metal atom are 3. This means that the hybridization will be
and the electronic geometry of the molecule will be trigonal planar.
Hence, the correct answer is Option D.
Answer:
1) positive
2) carbocation
3) most stable
4) faster
Explanation:
A common test for the presence of alcohols can be achieved using the Lucas reagent. Lucas reagent is a mixture of concentrated hydrochloric acid and zinc chloride.
The reaction of Lucas reagent reacts with alcohols leading to the formation of an alkyl chloride. Since the reaction proceeds via a carbocation mechanism, tertiary alcohols give an immediate reaction. Once a tertiary alcohol is mixed with Lucas reagent, the solution turns cloudy almost immediately indicating an instant positive reaction.
Secondary alcohols may turn cloudy within five minutes of mixing the solutions. Primary alcohols do not significantly react with Lucas reagent obviously because they do not form stable carbocations.
Therefore we can use the Lucas reagent to distinguish between primary, secondary and tertiary alcohols.