Chemistry College

When a mineral breaks along a weekly bonded plane it is called

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Answer 1

Answer: Cleavage

Explanation:

When a mineral breaks along a weekly bonded plane it is called cleavage

Related Questions

Identify each of the following orbitals, and determine the n and quantum numbers. Explain your answers.

Answers

(a) one radial node the Number of radial nodes = n - l - 1

And number of angular nodes = l

n = 3 and l = 1

Orbital is 3p.

(b) It has zero angular node hence s-orbital and there is 1 radial node . 1 = n - 0 - 1 ; n = 2 and l = 0

The orbital is 2s.

n = 3 and l = 2

Hence the orbital is 3dz².

What is radial node?

In atomic physics, a radial node is a point in space where the probability density of finding an electron in an atom is zero. It is a type of nodal plane that occurs in atomic orbitals, which are regions of space where electrons are most likely to be found.

Radial nodes occur in the radial distribution function of an atomic orbital, which describes the probability density of finding an electron at a given distance from the nucleus. The number of radial nodes in an atomic orbital is equal to n - l - 1, where n is the principal quantum number and l is the azimuthal quantum number.

Radial nodes represent regions of space where the radial wave function of the electron changes sign.

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Which of the following molecules is drawn in a conformation that has a proton and a leaving group anti-periplanar? H₂C, Br Ph. H CH3 Br H H₂C Br H₂C Ph H₂C CH3 H Ph H₂C, Br H Ph Save for Later CH3 CH3 CH3 CH3 CH3 Sul

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The molecule that is drawn in a conformation that has a proton and a leaving group anti-periplanar is H₂C, Br.

The A, B, C, and D bond angles of a molecule are referred to as anti-periplanar, or antiperiplanar, in organic chemistry. The dihedral angles of the A–B and C–D bonds in this conformer are larger than +150° or less than 150°. In textbooks, the term "anti-periplanar" is frequently used to refer to a strictly anti-coplanar structure with a 180° AB CD dihedral angle. The anti-periplanar functional groups will be 180° apart from one another and in a staggered configuration in a Newman projection of the molecule.

Conformation is an essential factor in predicting reactivity in organic molecules. The anti-periplanar conformation of a molecule is one that occurs when two atoms in a molecule are in the same plane and are separated by 180 degrees. In this case, the proton and leaving group are placed in a perpendicular plane to the atoms directly in between them. This is the most stable conformer of the molecule. A significant factor in predicting reactivity in organic molecules is conformation. In this case, the molecule H₂C, Br is drawn in a conformation that has a proton and a leaving group anti-periplanar.

Therefore, the correct option is H₂C, Br.

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match each substance correctly to the principal type(s) of intermolecular force(s) present, other than covalent bonding.

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Substance intermolecular force

CH2OH ---> Hydrogen bonding

CH3F --> Dipole-dipole forces

C3H8 --> Dispersion forces

CaCL2 --> Ionic bonding

The intermolecular force present in CH2OH is hydrogen bonding. The intermolecular force present in CH3F is Dipole-dipole forces. Ionic bonding is defined as a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions or between two atoms with sharply different electronegativities. It is the primary interaction occurring in ionic compounds. Hydrogen bonding results from the attractive force between a hydrogen atom covalently bonded to a very electronegative atom such as a N, O, or F atom and another very electronegative atom.

Dipole-dipole forces are defined as a attractive forces between the positive end of one polar molecule and the negative end of another polar molecule. Dispersion force is defined as a temporary attractive force that results when the electrons in two adjacent atoms occupy positions that make the atoms form temporary dipoles.

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The complete question is,

Match each substance correctly to the principal type(s) of intermolecular force(s) present, other than covalent bonding.

CH2OH Ionic bonding

CH3F Hydrogen bonding

C3H8 Dispersion forces

CaCL2 Dipole-dipole forces

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