Answer:
22.4L of one mole of any gas
or you can use PV=nRT
3.45*22.4=77.28
Explanation:
Answer:
F = 50 N
Explanation:
Given data:
Mass of car = 250 Kg
Acceleration of car = 0.20 m/s²
Force required = ?
Solution:
Formula:
F = m×a
F = applied force
m = mass
a = acceleration
Now we will put the values in formula.
F = 250 Kg × 0.20 m/s²
F = 50 Kg.m/s²
Kg.m/s² = N
F = 50 N
Answer:
1 strong acid
2 yes they are dangerous
Explanation:
Since nearly all of it is dissociated in water, it is called a strong acid.
2 yes Concentrated strong acids can cause severe and painful burns. The pain is due in part to the formation of a protein layer, which resists further penetration of the acid
So,
Formate has a resonating double bond.
In molecular orbital theory, the resonating electrons are actually delocalized and are shared between the two oxygens. So the carbon-oxygen bonds can be described as 1.5-bonds (option B). I'm not sure if option C is correct, however, because the likelihood of both delocalized electrons being in the area of one oxygen atom is less than 50%.<span />
A carboxylic acid is named in the IUPAC system by replacing the -e in the name of the parent alkane with -<u>oic acid</u>
<u></u>
<h3>What is carboxylic acid?</h3>
Carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.
Carboxylic acids are commonly identified by their trivial names. They often have the suffix -ic acid. IUPAC-recommended names also exist; in this system, carboxylic acids have an -oic acid suffix. For example, butyric acid (C3H7CO2H) is butanoic acid by IUPAC guidelines. For nomenclature of complex molecules containing a carboxylic acid, the carboxyl can be considered position one of the parent chain even if there are other substituents, such as 3-chloropropanoic acid. Alternately, it can be named as a "carboxy" or "carboxylic acid" substituent on another parent structure, such as 2-carboxyfuran.
Learn more about carboxylic acid
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