Answer:
Correct answers: 2 and 3
Explanation:
1- correct would be: Isolation of ibuprofen is not dangerous, but it is necessary because only one enantiomer has effect on interaction with biologic <em>diana</em>
<em>2: Correct! This property of diastereomeric salts (differing solubilities) is really useful for the isolation of the original enantiomers</em>
<em>3: Correct! we can only observe their properties, like polirized light rotation or separation in an assimetric column for chromatography.</em>
4: correct would be: diastereomeric salts do not rotate light, they have lost the property of anantiomers that originated them
This question is incomplete. Luckily, I found the same problem which is shown in the attached picture. To answer the question, we must know how the size and charge affect the lattice energy. The answer is: lattice energy increases with the increasing charge of the ions, and decreasing radius of the atoms.
<em>Therefore, the ranking would be: A < B < C</em>.
Answer: <u>Four</u>Explanation: Calcium Sulfide is an ionic compound made up of Ca²⁺ and S²⁻.
Ca²⁺ is formed as,
Ca → Ca²⁺ + 2 e⁻
These two electrons are accepte by Sulfur as,
S + 2 e⁻ → S²⁻
So, before accepting 2 electrons S was having six valence electrons, after accepting two electrons from Ca it has 8 electrons which are present in four pairs as shown below,
Answer:
The different structures are shown in the attachment.
I and II - structural isomers
I and III - Structural isomers
I and IV - structural isomers
II and III - structural isomers
II and IV - structural isomers
III and IV - stereoisomers
Explanation:
The knowledge of Isomerism is tested here; there are two types of isomerism ; structural and stereoisomerism.
- Structural Isomers have similar molecular and different double bond positioning, these occurs mostly in ALKENE FAMILY.
- Stereo-isomers have the same molecular formular and similar patterns but differ in their spatial arrangement. trans and cis are typical examples of stereo-isomers.
From the question; Relationship between I and II is that they are structural isomers since they have the same molecular formula, but different bond atom arrangement and infact they are the same compound.
- Relationship between I and III is that they are structural isomers with similar molecular formular but differ in the double bond position.
- Relationship between I and IV is that they are structural isomers with similar molecular formula but different double bond arrangement.
- Relationship between II and III is that they are structural isomers with similar molecular formular but different double bond position
- Relationship between II and IV is that they are also structural isomers with the same molecular formular but different double bond position.
- Relationship between III and IV is that they are stereo-isomers with same molecular formula but different spatial arrangement, hence cis and trans.
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