Compounds that have the same atoms (molecular formula) but different in the connectivity between the atoms are constitutional (formerly 'structural') isomers.

Isomers have the same chemical formulas, but different structures. They can be drastically different in structure, such as constitutional isomers, which differ in the way that certain groups are linked to a carbon back bone. They can be very subtly different as well, such as stereo isomers, which are almost completely same except for their biological activities and interactions with plane polarized light.

The isomers of ( C_6H_{14} ) include n-hexane, 2-methylpentane, 3-methylpentane, and 2,2-dimethylbutane. These isomers have different structural arrangements of carbon and hydrogen atoms, resulting in unique chemical properties.

Isomers in carbohydrates are molecules that have the same molecular formula but different structural arrangements. For example, glucose and fructose are isomers of each other. They have the same number of carbon, hydrogen, and oxygen atoms, but their structures differ, resulting in different chemical and biological properties.

The trisoxalatochromate ion has two isomers: fac-trisoxalatochromate and mer-trisoxalatochromate. In fac-isomer, the oxalate ligands are arranged in a facial manner, whereas in the mer-isomer, the oxalate ligands are arranged in a meridional manner around the chromium central atom.

I assume you mean "isotopes" instead of isomers. The term "isotope" refers to the relationship between two or more atoms of the same element which have different atomic masses; therefore, they have a different number of neutrons. Carbon-12 and Carbon-14 are isotopes: same element, different masses. Carbon-12 is more prevalent and more stable, but C-14 is still "normal."

P.S. "Isomers" have to do with the "handedness" of molecules. Some are right-handed and others left. It's seen mostly in organic chemistry. Our bodies use Right-handed glucose (D-glucose), but left-handed amino acids (L-alanine, e.g.).

Nonane has a total of 75 isomers, which includes straight chain isomers, branched chain isomers, and cyclic isomers.

1-bromobutane

2-bromobutane

1-bromo 2-methylpropane

2-bromo 2-methylpropane

Three

Three types of isomers are structural isomers (different connectivity of atoms), stereoisomers (same connectivity but different spatial arrangement), and conformational isomers (different spatial arrangement due to rotation around single bonds).

hydrocarbons, they are called isomers

There are two isomers for dibromopropane: 1,2-dibromopropane and 2,2-dibromopropane.

E isomers are entgegen isomers. The groups with the highest priority are located on opposite sides of a double bond.

Decane has 75 isomers, including straight-chain, branched-chain, and cyclic isomers.

Yes, RNA can have isomers. Isomers are molecules with the same molecular formula but different structural arrangements. In the case of RNA, isomers can arise due to differences in the sequence or arrangement of nucleotides within the RNA molecule.

Organic compounds with the same molecular formula but different structural formulas are classified as structural isomers. These isomers have different arrangements of atoms within their structures, which can lead to differences in their physical and chemical properties. Examples of structural isomers include chain isomers, functional group isomers, and positional isomers.

Constitutional isomers have different molecular structures, while conformational isomers have the same structure but differ in the arrangement of atoms in space.

Isomers are compounds with the same chemical formula but different structures. They can have different physical and chemical properties due to their unique arrangement of atoms. Examples include structural isomers, geometric isomers, and optical isomers.

Three isomers of C2HfClBr are possible.

The isomers for C9H20 are nonane, iso-nonane, and neo-nonane. These isomers have different structures, leading to unique chemical and physical properties.

There are a total of three structural isomers of C7H16 that have no secondary hydrogen atoms. These isomers are 2-methylhexane, 3-methylhexane, and 2,2-dimethylpentane.

In organic chemistry, ortho, meta, and para isomers are types of positional isomers that differ in the placement of substituents on a benzene ring. Ortho isomers have substituents on adjacent carbons, meta isomers have substituents on carbons separated by one carbon, and para isomers have substituents on opposite carbons. These differences in positioning can affect the physical and chemical properties of the isomers.

This is an incomplete question. Isomers of what? What kind of isomers? You need to learn more about the topic before you submit a question to a public forum.

Optical isomers are isomers of molecules which are non-superimposible. They have a left hand and a right hand and this is how you distinguish between them.

C3H4O can have two isomers: propynal and cyclopropanone.

The isomers of C4H8O are butanal, 2-methylpropanal, and 2-butanone.

Information about isomers can be found in all chemistry text books. Isomers are compounds which have the same molecular layout but have a different structure.

Cis and trans isomers of cyclohexane differ in the spatial arrangement of their substituent groups. In cis isomers, the substituent groups are on the same side of the ring, while in trans isomers, they are on opposite sides. This difference affects the physical and chemical properties of the isomers.

Isomers are molecules with the same chemical formula but different structures. Due to their different structures, isomers can have different boiling points.

Isomers.

If they're isomers, they by definition have the same molecular formula.

Well, honey, C6H12Cl2 has three isomers. You've got your 1,1-dichlorohexane, 1,2-dichlorohexane, and 1,6-dichlorohexane. So, there you have it, three isomers strutting their stuff in the world of organic chemistry.

Molecules with the same molcular formulae but differing structural formulae are called isomers.

There are two types of geometric isomers possible in octahedral complex ions: cis and trans isomers. For a complex with six different ligands, there can be a maximum of 30 different cis and trans isomers.

There are three isomers for C6H4Cl2: 1,2-dichlorobenzene, 1,3-dichlorobenzene, and 1,4-dichlorobenzene. These isomers have different arrangements of the chlorine atoms on the benzene ring.

Pentane has three isomers: n-pentane, isopentane, and neopentane. Isomers are molecules that have the same molecular formula but different structural arrangements. In the case of pentane, these isomers differ in the way the carbon atoms are connected to each other.

There are three isomers that can be constructed for C3H6I2. These include 1,1-diiodopropane, 1,2-diiodopropane, and 2-iodopropane.

The prefix used for isomers is "iso-". It indicates that the compounds have the same molecular formula but differ in structure or arrangement of atoms.

They are called isomers. Isomers may be structural isomers (e.g. 1-propanol and isopropanol) or stereoisomers (e.g. L-aspartic acid and D-aspartic acid).

Isomers are organic compounds that have the same molecular formula but different structural arrangements of atoms. These structural isomers can differ in the order the atoms are connected, leading to different properties and reactivities. An example of structural isomers are n-pentane and isopentane, both with the molecular formula C5H12.

Isomers of an alkane with the same molecular formula have different structural arrangements of atoms, leading to distinct chemical and physical properties. Examples include different branching patterns in chain isomers or different spatial arrangements in geometric isomers.

The different isomers of C4H8O are butanal, 2-methylpropanal, and 2-butanone.

C3H12 can have two different isomers: n-propane, which is a straight chain molecule, and isobutane, which is a branched molecule.

There are 5 isomers of C6H12C12, namely n-hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, and cyclohexane.

There are a total of 16 possible isomers of a D-ketohexofuranose. This includes aldohexose isomers as well as ketohexose isomers. The structural diversity arises from variations in the arrangement of hydroxyl (-OH) groups and the position of the carbonyl group.

Para and ortho isomers are types of structural isomers in organic chemistry. The main difference between them is the position of substituents on a benzene ring. In para isomers, the substituents are located opposite each other on the benzene ring, while in ortho isomers, the substituents are adjacent to each other on the ring.

The dehydration of cyclohexanol can form two isomers: cyclohexene and cyclohexadiene. These isomers result from different locations of the double bond formed during the dehydration process.

This compound (dibromomethane) has only one form. It does not form isomers .

The isomers of C6H10 are:

1. Cyclohexane
2. Methylcyclopentane
3. 1-Hexene
4. Cyclohexene
5. 2-Hexene

There are three isomers of C3H6I2: 1,1-diiodopropane, 1,2-diiodopropane, and 2,2-diiodopropane.