Thiols are sulfur analogues of alcohols, containing an SH group in place of the OH group. When naming a thiol, we follow the same rules we discussed earlier for the IUPACnomenclature rules for alcohols, with the focus on giving the carbon bonded to the SH group the lowest locant.

This would be a brief summary for naming a thiol:

Step 1. Identify the parent chain.

Step 2. Identify the substituents.

Step 3. Number the parent chain, giving the carbon bonded to the SH group the lowest locant

Step 4. Put everything together, having the substituents in alphabetical order.

The presence of the SH group is identified bychanging the parent suffix from “e” to “thiol”:

For simple thiols, the common name can be derived by naming the alkyl group connected to the SH and adding the word mercaptan:

If it is a branched molecule, choose theparent chain such that it is thelongest carbon chain containing the carbon atom connected to the SH group:

TheSH group has a higher priority than alkyl substituents or π bonds. Therefore, you need to number the parent chain such that theSH gets the lowest possible number:

If theSH group is connected to a chiral center, you will also need to include theabsolute configuration at the beginning of the name. Also, if there is a double, theEandZ configuration should be addressed when applicable:

When naming acyclic thiol, start numbering the ringbeginning with the carbon connected to the SH group. This rule always puts the SH group at C1; therefore, the “1” is usually omitted from the name:

When other groups are present on the ring, it is numbered clockwise or counterclockwisedepending on which direction gives the next substituent the lower number:

Thiols can also be identified by their common name,mercaptans, which literally means mercury capturing. This comes from the discovery of their strong affinity to heavy metal cations such as arsenic, which leads to forming strong complexes with them:

Compounds Where the Thiols areNot the Highest Priority

If the molecule contains a functional group with ahigher priority than the thiol, the latter is mentioned as a substituent. The molecule in this case gets the suffix from the other functional group, while the prefix “mercapto” is used to mention the SH substituent.

For example, the hydroxyl takes precedence over the thiol, and therefore, we use the suffix “ol” andprefix mercapto:

 Alternatively, the SH group may be indicated by the prefix “sulfanyl”.

For determining thepriorities of functional groups in a molecule, refer to the corresponding table, which can be foundhere.

Naming Sulfides

Sulfides are the sulfur analogs of ethers and are, therefore, also calledthioethers.

Just likeethers, sulfides are named by both common and systematic nomenclature of the IUPAC rules. The common names are used for sulfides with simple alkyl groups. To do this, we first identify the alkyl groups and arrange them in alphabetical order, followed by the word “sulfide”.

For example,

The molecules above are examples of unsymmetrical sulfides i.e., different alkyl groups are bridged with the sulfur.

If the groups are identical – symmetrical sulfides, the prefix “di” is added. For example,

The Systematic Nomenclature of Sulfides

The systematic nomenclature is used for sulfides with complex substituents. The idea here is to treat one of the alkyl groups with the sulfur as a substituent connected to a parent chain. This substituent is named as “alkylsulfanyl” or “alkylthio”, shown inparentheses. Theparent chain is determined just like we always do, based on the longest carbon chain.

For example,

Check Also

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• Preparation of Alcohols via Substitution or Addition Reactions
• Reaction of Alcohols with HCl, HBr, and HI Acids
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• SOCl₂ and PBr₃ for Conversion of Alcohols to Alkyl Halides
• Alcohols in Substitution Reactions  Practice Problems
• POCl₃ for Dehydration of Alcohols
• Dehydration of Alcohols by E1 and E2 Elimination
• The Oxidation States of Organic Compounds
• LiAlH4 and NaBH4 Carbonyl Reduction Mechanism
• Alcohols from Carbonyl Reductions – Practice Problems
• Grignard Reaction in Preparing Alcohols with Practice Problems
• Grignard Reaction in Organic Synthesis with Practice Problems
• Protecting Groups For Alcohols in Organic Synthesis
• Oxidation of Alcohols: PCC, PDC, CrO₃, DMP, Swern, and All of That
• Diols: Nomenclature, Preparation, and Reactions
• NaIO4 Oxidative Cleavage of Diols
• The Pinacol Rearrangement
• The Williamson Ether Synthesis
• Alcohol Reactions Practice Problems
• Reactions of Thiols
• Alcohols Quiz – Naming, Preparation, and Reactions
• Reactions Map of Alcohols