Answer: The correct answer is "B" two bonding domains(or bonding pairs) or two non bonding domains(or lone pairs)
Explanation:
Molecular geometry/structure is a three dimensional shape of a molecule. It is basically an arrangement of atoms in a molecule.It is determined by the central atom, its surrounding atoms and electron pairs.According to VSEPR theory, there are 5 basic shapes of a molecule: linear, trigonal planar, tetrahedral, trigonal bipyramidal and octahedral.
A)Four bonding domains and zero non bonding domains: shape is tetrahedral and bond angle is 109.5°
B)Two bonding domains and two non bonding domains(lone pairs): shape is bent and bond angle is 104.5°
C)Three bonding domains and one non bonding domain: shape is trigonal pyramidal and bond angle is 107°
D)Two bonding domain and zero non bonding domain: shape is linear and bond angle is 107°
E)Two bonding domain and one non bonding domain: bent shape and bond angle is 120°
F)Three bonding domains and zero nonbonding domain: shape is trigonal planar and bond angle is 120°
Hence Two bonding domains and two non bonding domains have the smallest bond angle.
Burrows, tracks, coprolites, nests and footprints are examples of traces that can be found in a fossil.
Answer:
False
Explanation:
The statement is implying that this is the only way to obtain a salt. Any ionic compound is a salt. For example, NaCl (table salt) is an ionic compound. It is the combination of a nonmetal (Cl) and a metal (Na).
Atmosphere. You can think of the atmosphere as the outer shell for earth.
Ethyl acetate and methyl benzoate combination of reactants will produce ethyl 3-phenyl-3-oxopropanoate when treated first with an alkoxide and then with a diluted aqueous acid
<h3>Ethyl acetate</h3>
One of the most straightforward carboxylate esters is ethyl acetate. The simplest is methyl formate, a former Molecule of the Week. Most people enjoy the taste and aroma of the colorless liquid's sweet, fruity scent.
Ethyl acetate was initially created by combining ethanol and acetic acid, as one might anticipate. The process was the traditional Fischer esterification, which dates back to 1895 and is catalyzed by an acid. This commercial synthesis is still the most popular. A different approach is the Tishchenko reaction, in which acetaldehyde disproportionately reacts with base to form alcohol and acid, which subsequently esterify naturally.
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