Check the box under each compound that exists as a pair of cis/trans isomers. If none of them do, check the none of the above box under the table. HỌ—CH=CH2 CH3-CH=CH₂ none of the above CH3 CH3 C CH₂ CH3 CH3 НО C=C -OH X S
Classes Of Functional Groups
Organic Chemistry deals mostly with carbon and hydrogens, also called hydrocarbons, but those groups which replace hydrogen and bonds with carbon to give a characteristic nature, unique of their own, to the hydrocarbon they are attached to, are called functional groups. All the compounds belonging to a functional group undergo reactions in a similar pattern and are known to have similar physical and chemical properties.
Characteristics Of Functional Groups
In organic chemistry, we encounter a number of special substituent groups which are attached to the hydrocarbon backbone. These groups impart certain characteristics to the molecule of which it is a part of and thus, become the highlight of that particular molecule.
IUPAC Nomenclature
In Chemistry, IUPAC stands for International Union of Pure and Applied Chemistry which suggested a systematic naming approach for the organic and inorganic compounds, as in the beginning stage of nomenclature one single chemical compound was named in many ways by which lead to confusion. The need for this approach aroused as the number of chemical compounds newly discovered were increasing (approximately 32 million compounds) and the basic concept of nomenclature i.e. the trivial nomenclature and the derived system of nomenclature failed to overcome the challenge. It is an important task to name a chemical compound systematically and unambiguously which reduces lots of confusion about the newly reported compounds.
![Check the box under each compound that exists as a pair of cis/trans isomers. If none of them do, check the none of the above box under the table.
HỌ—CH=CH2
CH3-CH=CH₂
0
none of the above
CH3
CH3 C CH ₂
HO
0
CH3 CH3
C C -OH
X
S](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F01c4c03f-20b0-4034-9a31-8f142f99d675%2Fed066c3c-9aa8-4575-8d61-e970a1edc36e%2Fp01t2ub_processed.jpeg&w=3840&q=75)
![=
O PRINCIPLES OF ORGANIC CHEMISTRY
Identifying rigid parts of an acyclic organic molecule
In the actual molecule of which this is a Lewis structure, which of the labeled distances can change?
marked
10
H
O
H
B
G1C
F
H
A
N
E
unmarked
C
O
H
List all the distances that can change. For example, suppose all the distances were measured at a certain time, and again 0.1s later. If distance A might
be 50% bigger or smaller the second time, but all the other distances are certain to be the same, you should write "A". If A and B might be different
the second time, but no other distances, you would write "A, B". And so on.
Note for advanced students: you can assume the molecule is dissolved in an appropriate solvent at room temperature.
00....
X
90/5
You can click the "unmarked" tab to see the molecule without any of the distances marked.
5
Ja](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F01c4c03f-20b0-4034-9a31-8f142f99d675%2Fed066c3c-9aa8-4575-8d61-e970a1edc36e%2F3wvfogu_processed.jpeg&w=3840&q=75)
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