酮
酮与氰根发生亲核加成生成羟基腈,构成另一条由羰基化合物出发的路线。
- 官能团
- C=O
- Also known as
- alkanones, ketone, carbonyl compounds
概览
Carbonyl compounds with an internal C=O group.
A ketone has two carbon groups bonded to the carbonyl carbon. Reduction gives a secondary alcohol. Ordinary aldehyde oxidation tests usually leave simple ketones unchanged; this is a condition-dependent contrast, not a claim that ketones can never be oxidised.
Identifiers
- 官能团
- C=O
- Also known as
- alkanones, ketone, carbonyl compounds
化学标识符
- SMILES
- CC(=O)C
性质
- 氧化的适用边界
- 强氧化条件可能断裂碳碳键,并非简单生成保留原碳骨架的羧酸。
- 碘仿反应的适用边界
- 只有甲基酮子类具有常规碘仿反应所需的 CH3CO- 结构。
Diagnostic tests
2,4-二硝基苯肼羰基试验
- 试剂
- 2,4-二硝基苯肼
- 条件
- 室温
- Positive observation
- 橙色沉淀
- Negative observation
- 无橙色沉淀
- Interpretation
- 醛或酮与此试剂形成沉淀;酯、羧酸及酰胺的羰基反应性另行区分。
- 适用范围
- 醛和酮可形成 2,4-二硝基苯腙。
- 来源说明
- 醛与酮均可呈阳性,结合衍生物熔点或光谱比较。
- 证据
- 教材核心内容
Related compounds
Connected reactions
- Cyanohydrin formation: Ketones → Hydroxynitriles
氰根与酮加成生成羟基腈,为有机反应网络增加另一条羰基路线。
- Oxidation: Alcohols → Ketones
仲醇氧化生成酮。
- Oxidation: Secondary alcohols → Ketones
仲醇氧化生成酮。
- Reduction: Ketones → Secondary alcohols
酮还原生成仲醇。
- Grignard addition co reactant: Ketones → Tertiary alcohols
酮与格氏试剂反应,经酸性后处理得到叔醇。
参考文献
- Organic Chemistry: Oxidation of Aldehydes and KetonesJohn McMurry · OpenStax Organic Chemistry · 2023
Supports functional-group chemistry used to curate the linked examples. Checked 2026-09-16; named examples are applications of textbook scope, without claimed experimental yields.
- Pearson Edexcel International Advanced Level Chemistry Practical GuidePearson Education Limited · Pearson qualifications · 2018
Official Pearson practical guidance for organic qualitative tests, including bromine water, acidified dichromate, silver nitrate, carbonyl reagents and the iodoform reaction.
- Pearson Edexcel Level 3 Advanced GCE in Chemistry specificationPearson Education Limited · Pearson qualifications · 2024
Supports the textbook-core organic reaction routes used for displayed route and mechanism content.
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