The coordination compounds that exhibit cis and trans isomer has to be identified. Concept Introduction: Isomers: The compounds with same molecular formula but differ in the arrangement of the atom are said to be isomers. Stereo isomers: Stereo isomers are the isomers that have same molecular formula but differ in spatial arrangement of atoms. Stereo isomers can be sub divided into two groups, Optical isomers Geometrical isomers Geometric isomers: If there is restricted rotation in a molecule there arise geometric isomerisms. Geometric isomers are also known as Cis- trans isomerism. If the two atoms locked in same side of the molecule then it is called as cis isomers. If the two atoms locked in opposite side of the molecule then it is called as trans isomers.

Question

Want to see the full answer?

Answer 1

Question

Chapter 9, Problem 9C.14E

Interpretation Introduction

Interpretation:

The coordination compounds that exhibit cis and trans isomer has to be identified.

Concept Introduction:

Isomers:

The compounds with same molecular formula but differ in the arrangement of the atom are said to be isomers.

Stereo isomers:

Stereo isomers are the isomers that have same molecular formula but differ in spatial arrangement of atoms. Stereo isomers can be sub divided into two groups,

Optical isomers

Geometrical isomers

Geometric isomers:

If there is restricted rotation in a molecule there arise geometric isomerisms. Geometric isomers are also known as Cis- trans isomerism.

If the two atoms locked in same side of the molecule then it is called as cis isomers.

If the two atoms locked in opposite side of the molecule then it is called as trans isomers.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Arrange the solutions in order of increasing acidity. (Note that K (HF) = 6.8 x 10 and K (NH3) = 1.8 × 10-5) Rank solutions from least acidity to greatest acidity. To rank items as equivalent, overlap them. ▸ View Available Hint(s) Least acidity NH&F NaBr NaOH NH,Br NaCIO Reset Greatest acidity

1. Consider the following molecular-level diagrams of a titration. O-HA molecule -Aion °° о ° (a) о (b) (c) (d) a. Which diagram best illustrates the microscopic representation for the EQUIVALENCE POINT in a titration of a weak acid (HA) with sodium. hydroxide? (e)

Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single file upload below: Review of this week's reaction: H₂NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H₂O ---> H₂NC(=NH)N(CH3)CH2COOH (creatine) Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts) Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts) Q9. Explain with drawing why the C-N bond shown in creatine structure below can or cannot rotate. (3 pts) NH2(C=NH)-N(CH)CH2COOH This bond Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem Q9 is valid). (4 pts) Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should be ready to understand the first half of one of the Grignard reactions presented in a past…