The options for given question are as follow,
1) Methane molecules show hydrogen bonding.
<span>2) Ammonia molecules show hydrogen bonding. </span>
<span>3) Methane has stronger hydrogen bonding than ammonia. </span>
<span>4) Both the compounds do not show hydrogen bonding. </span>
<span>5) Both the compounds have strong hydrogen bonding.
</span>
Answer:
Correct answer is Option-2 (Ammonia molecules show hydrogen bonding).
Explanation:
Hydrogen bond interactions are formed when a partial positive hydrogen atom attached to most electronegative atom of one molecule interacts with the partial negative most electronegative element of another molecule. So, in Ammonia hydrogen gets partial positive charge as nitrogen is highly electronegative. While the C-H bond in Methane is non-polar and fails to form hydrogen bond interactions.
Answer:
300000Pa or 3×10^5 Pa
Explanation:
Since the problem involves only two parameters of volume and pressure, the formula for Boyle's law is suitably used.
Using Boyle's law
P1V1 = P2V2
P1 is the initial pressure = 1.5×10^5Pa
V1 is the initial volume = 0.08m3
P2 is the final pressure (required)
V2 is the final volume = 0.04 m3
From the formula, P2 = P1V1/V2
P2 = 1.5×10^5 × 0.08 ÷ 0.04
= 300000Pa or 3×10^5 Pa.
Answer:
1. The product has a higher Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate.
2. False
3. True
Explanation:
In chromatography, there is a stationary phase and a mobile phase. The ratio of the distance moved by a component and the distance moved by the solvent gives the retention factor (Rf).
Since silica gel is a polar solvent, it will retain the more polar product methyl m-nitrobenzoate compared to the methyl benzoate starting material.
In comparing the electrophillic aromatic substitution of m-nitrobenzoate and methyl benzoate, we must remember that the presence of electron withdrawing groups (such as -NO2 and -CHO) on the aromatic compound deactivates the compound towards electrophillic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substition
I believe it would be a compound.
I believe a hydrochloric gas will be let off
