Answer:
number of carbon-carbon single (C - C) bonds: 1
number of carbon-hydrogen single (C H) bonds: 5
number of nitrogen-hydrogen sing le (N H) bonds:2
number of lone pairs: 1
Explanation:
Ethanamine is a colourless gas having a strong 'ammonia- like' odour. It contains the -NH2 group which makes it an amine. It contains one carbon-carbon bond, five carbon-hydrogen bonds and two nitrogen-hydrogen bonds.
Nitrogen, being sp3 hybridized in the compound has a lone pair of electrons localized on one of the sp3 hybridized orbitals of nitrogen while one sp3 hybridized orbital of nitrogen is used to form a carbon-nitrogen bond. The other two sp3 hybridized orbitals on nitrogen are used to form the two nitrogen-hydrogen bonds.
Answer:
14) The edge dislocation is more plastic than the screw dislocation
15) So as to form kinks that are fast moving
Explanation:
14) Edge and screw dislocations are the two main types of mobile dislocations
The three dimensional core of the screw dislocation prevents the slipping of the layers (one over the other) in a BCC metal such that kinks are required to be formed first by thermal activation (heating) in order. The kinks are edge dislocation that move such that the screw dislocation moves forward
Hence, the edge dislocation is more plastic than the screw dislocation
15) The three dimensional structure of a screw dislocation acts like a wedge which resists the slipping of the layers in the BCC structure such that the screw dislocation needs to be highly thermally activated forming kinks before the surrounding layers can move.
<span>• Benzene has the formula of C6H<span>6 </span>whereas cyclohexane has the formula of C6H<span>12.
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Benzene is an aromatic compound but cyclohexane is not aromatic.
Benzene is an unsaturated molecule, but cyclohexane is saturated.
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Carbon atoms in the benzene ring have sp2 hybridization where carbon atoms in the cyclohexane have sp3 hybridization.</span>
Benzene has a planar structure whereas cyclohexane has chair conformations.<span>
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Answer:
Explanation has been given below.
Explanation:
- Chloroform has three polar C-Cl bonds. Methylene chloride has two polar C-Cl bonds. So it is expected that chloroform should be more polar and posses higher dipole moment than methylene chloride.
- Two factors are liable for the opposite trend observed in dipole moments of methylene chloride and chloroform.
- First one is the number of hyperconjugative hydrogen atoms present in a molecule. Hyperconjugation occurs with vacant d-orbital of Cl atom. Hyperconjugation amplifies charge separation in a molecule resulting higher dipole moment.
- Methylene chloride has two hyperconjugative hydrogen atoms and chloroform has one hyperconjugative hydrogen atom.Therefore methylene chloride should have higher charge separation as compared to chloroform.
- Second one is induction of opposite polarity in a C-Cl bond by another C-Cl bond in a molecule. Higher the opposite induction of polarity, lower the charge separation in a molecule and hence lower the dipole moment of a molecule.
- Chloroform has three C-Cl bonds and methylene chloride has two C-Cl bonds. Therefore opposite induction is higher for chloroform resulting it's lower dipole moment.
