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Group 14 hydride

Group 14 hydride is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Group 14 hydride rather than just read about it. In short: Group 14 hydrides are chemical compounds composed of hydrogen atoms and group 14 atoms (the elements of group 14 are carbon, silicon, germanium, tin, lead and flerovium). Tetrahydrides The tetrahydride series has the chemical formula XH4, with X representing any of the carbon family.

Group 14 hydride — main illustration
Group 14 hydride — illustration

Key takeaways

  • Group 14 hydride belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Group 14 hydride to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Group 14 hydride from memory before moving on to harder problems.

Reference excerpt

Group 14 hydrides are chemical compounds composed of hydrogen atoms and group 14 atoms (the elements of group 14 are carbon, silicon, germanium, tin, lead and flerovium).

Tetrahydrides The tetrahydride series has the chemical formula XH4, with X representing any of the carbon family. Methane is commonly the result of the decomposition of organic matter and is a greenhouse gas. The other hydrides are generally unstable, poisonous metal hydrides. They take on a pyramidal structure, and as such are not polar molecules like the other p-block hydrides. Unlike other light hydrides such as ammonia, water and hydrogen fluoride, methane does not exhibit any anomalous effects attributed to hydrogen bonding, and so its properties conform well to the prevailing trend of heavier group 14 hydrides.

Hexahydrides This series has the chemical formula X2H6. Ethane is commonly found alongside methane in natural gas. The other hydrides of the chemical formula X2H6 are less stable than the corresponding tetrahydrides XH4, and they are more and more less stable as X goes from carbon (ethane C2H6 is stable) down to lead (or flerovium) in the periodic table (diplumbane Pb2H6 is unknown).

Higher group 14 hydrides All straight-chain saturated group 14 hydrides follow the formula XnH2n+2, the same formula for the alkanes.

Many other group 14 hydrides are known. Carbon forms a huge variety of hydrocarbons (among the simplest alkanes are methane CH4, ethane C2H6, propane C3H8, butane C4H10, pentane C5H12 and hexane C6H14, with a wide range of uses. There is also polyethylene (CH2)n, where n is very large, a stable hydrocarbon polymer, the most commonly produced plastic. Hydrocarbons also include alkenes, which contain a double bond between carbon atoms (e.g. ethylene H2C=CH2), alkynes, which contain a triple bond between carbon atoms (e.g. acetylene H−C≡C−H), cyclic and branched hydrocarbons (e.g. cyclohexane C6H12, limonene C10H16, which is a cyclic hydrocarbon with double bonds between carbon atoms, and neopentane C(CH3)4, which is a branched hydrocarbon), as well as aromatic hydrocarbons such as benzene C6H6 and toluene C6H5−CH3), whose study forms the core of organic chemistry. Alongside hydrogen, carbon can form compounds with the chemically similar halogens, forming haloalkanes. The simplest of this series, the halomethanes, contain compounds such as dichloromethane CH2Cl2, chloroform CHCl3 and iodoform CHI3. Other such important chemicals include vinyl chloride H2C=CHCl, which is used in the production of PVC. The other group 14 elements have a lower tendency to catenate. Hydrosilicons (binary silicon-hydrogen compounds), a silicon analogs of hydrocarbons, such as silanes SinH2n+2 are known for n = 1–8, in which thermal stability decreasing as n increases (e.g. silane SiH4 and disilane Si2H6), as are cyclosilanes (e.g. cyclopentasilane Si5H10 and cyclohexasilane Si6H12). They are very reactive, pyrophoric colourless gases or volatile liquids. Their volatility is intermediate between the alkanes and the germanes. Unsaturated silanes, the silenes and silynes, have been characterized spectroscopically. The first members of each respectively are disilene H2Si=SiH2 and disilyne H−Si≡Si−H, the silicon analogues of ethylene and acetylene respectively. The first five hydrogermaniums GenH2n+2 are known and are fairly similar to the hydrosilicones, e.g. germane GeH4 and digermane Ge2H6. They are germanium analogues of alkanes. Stannane SnH4, a strong reducing agent slowly decomposes at room temperature to tin and hydrogen gas, and is decomposed by concentrated aqueous acids or alkalis; distannane, Sn2H6 is still more unstable, and longer hydrostannums (hydrotins) are unknown. Stannane and distannane are tin analogues of methane and ethane respectively. Plumbane PbH4 is very poorly characterised and is only known in trace amounts: even at low temperatures, synthesis methods that yield the other MH4 compounds fail to give PbH4. No other hydroplumbums (hydroleads) are known. However, some substituted diplumbanes, with a general chemical formula R3Pb−PbR3 are more stable, where the R groups are organyl. Compounds containing hydrogen and multiple group 14 elements are known, one of the most famous of these being tetraethyllead Pb(CH2CH3)4 which contains carbon and lead. The other examples are methylsilane H3C−SiH3 which contains carbon and silicon, tris(trimethylsilyl)germanium hydride ((CH3)3Si)3GeH which contain carbon, silicon and germanium, silylgermane or germylsilane H3Si−GeH3 which contains silicon and germanium, and hexaphenyldiplumbane (C6H5)3Pb−Pb(C6H5)3 which contains carbon and lead.

See also Methylene CH2 Methylidyne CH Titanium(IV) hydride TiH4, a structural analog of the group 14 tetrahydrides Zirconium hydride ZrH4 and others Zirconium(II) hydride ZrH2 Uranium(IV) hydride UH4

References

Bibliography Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.

Illustrations

Group 14 hydride illustration
Group 14 hydride illustration
Group 14 hydride illustration
Group 14 hydride illustration
Group 14 hydride illustration

Worked examples

Example 1 — a first encounter with Group 14 hydride

Start with the simplest possible case. Write down what Group 14 hydride claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Group 14 hydride before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Group 14 hydride ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Group 14 hydride

In research
Group 14 hydride appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Group 14 hydride in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Group 14 hydride is common in secondary-school and first-year university syllabi. It links to neighbouring topics Hydrides, Hydrogen compounds, so understanding it makes those chapters shorter.
In everyday life
Look for Group 14 hydride outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Group 14 hydride in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Group 14 hydride means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Group 14 hydride out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Group 14 hydride in simple terms?

Group 14 hydrides are chemical compounds composed of hydrogen atoms and group 14 atoms (the elements of group 14 are carbon, silicon, germanium, tin, lead and flerovium). Tetrahydrides The tetrahydride series has the chemical formula XH4, with X representing any of the carbon family.

Why does Group 14 hydride matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Group 14 hydride?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Group 14 hydride.

Tags

  • Hydrides
  • Hydrogen compounds

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