Chemical Properties of Phosphine and Introduction to Organic Chemistry

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Vocabulary practice flashcards covering the chemical properties, preparation methods, reactions, and uses of phosphine, along with fundamental concepts, history, and comparison of organic and inorganic compounds.

Last updated 11:31 AM on 10/6/26
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21 Terms

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Basic Nature of Phosphine (PH3PH_3)

Phosphine is basic in nature, but less basic than ammonia (NH3NH_3). It reacts with water to form phosphonium hydroxide (PH4OHPH_4OH) and hydroxide ions (OH−OH^-).

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Phosphonium Salt Formation

The reaction of phosphine (PH3PH_3) with acids to form phosphonium salts, such as PH3+HCl→PH4ClPH_3 + HCl \rightarrow PH_4Cl (Phosphonium chloride) and PH3+HBr→PH4BrPH_3 + HBr \rightarrow PH_4Br (Phosphonium bromide).

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Preparation of Phosphine from Calcium Phosphide

Phosphine gas is prepared by reacting calcium phosphide with water: Ca3P2+6H2O→3Ca(OH)2+2PH3↑Ca_3P_2 + 6H_2O \rightarrow 3Ca(OH)_2 + 2PH_3\uparrow

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Preparation of Phosphine from Phosphonium Iodide

Phosphine gas is obtained by reacting phosphonium iodide with potassium hydroxide: PH4I+KOH→PH3↑+KI+H2OPH_4I + KOH \rightarrow PH_3\uparrow + KI + H_2O

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Preparation of Phosphine from White Phosphorus

Phosphine gas is obtained by heating white phosphorus with sodium hydroxide and water: P4+3NaOH+3H2O→PH3↑+3NaH2PO2P_4 + 3NaOH + 3H_2O \rightarrow PH_3\uparrow + 3NaH_2PO_2

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Reducing Property of Phosphine (PH3PH_3)

Phosphine acts as a powerful reducing agent that reduces heavy metal salt solutions into metallic phosphides or oxides, which subsequently decompose into corresponding pure metals upon standing or heating.

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Reaction of Phosphine with Copper Sulfate (CuSO4CuSO_4)

When PH3PH_3 is passed through a CuSO4CuSO_4 solution, it reduces CuSO4CuSO_4 to a black precipitate of cupric phosphide (Cu3P2Cu_3P_2), which decomposes on heating into copper metal: 4PH3+6CuSO4→2Cu3P2+6H2SO44PH_3 + 6CuSO_4 \rightarrow 2Cu_3P_2 + 6H_2SO_4 and 2Cu3P2→6Cu+P42Cu_3P_2 \rightarrow 6Cu + P_4

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Reaction of Phosphine with Silver Nitrate (AgNO3AgNO_3)

When PH3PH_3 is passed through an AgNO3AgNO_3 solution, it reduces AgNO3AgNO_3 into a black precipitate of silver phosphide (Ag3PAg_3P), which decomposes on standing into silver metal: PH3+3AgNO3→Ag3P↓+3HNO3PH_3 + 3AgNO_3 \rightarrow Ag_3P\downarrow + 3HNO_3 and 4Ag3P→12Ag+P44Ag_3P \rightarrow 12Ag + P_4

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Reaction of Phosphine with Oxygen

Phosphine reacts with oxygen to form phosphoric acid (H3PO4H_3PO_4) in limited oxygen (PH3+2O2→H3PO4PH_3 + 2O_2 \rightarrow H_3PO_4) or phosphorus pentoxide (P2O5P_2O_5) in excess oxygen.

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Reaction of Phosphine with Chlorine

Phosphine reacts with chlorine to produce phosphorus trichloride (PH3+3Cl2→PCl3+3HClPH_3 + 3Cl_2 \rightarrow PCl_3 + 3HCl) or phosphorus pentachloride (PH3+4Cl2→PCl5+3HClPH_3 + 4Cl_2 \rightarrow PCl_5 + 3HCl), depending on the amount of chlorine used.

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Holmes Signal

A signal provided to ships using containers of calcium carbide (CaC2CaC_2) and calcium phosphide (Ca3P2Ca_3P_2), which react with water to release acetylene (C2H2C_2H_2) and phosphine (PH3PH_3), producing a bright flame and smoke.

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Smoke Screen Use of Phosphine

Phosphine (PH3PH_3) is used to create smoke screens in war due to its poisonous property.

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Organic Chemistry (Modern Definition)

The branch of chemistry that deals with the study of hydrocarbons and their derivatives.

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Organic Compounds

Hydrocarbons and their derivatives containing covalently bonded carbon atoms as an essential element, such as methanol (CH3OHCH_3OH), chloroform (CHCl3CHCl_3), ethene (CH2=CH2CH_2=CH_2), and vinyl chloride (CH2=CH−ClCH_2=CH-Cl).

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Vital Force Theory

A historical theory stating that organic compounds are formed only by living organisms (plants and animals) under the influence of a vital force and cannot be synthesized in the laboratory.

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Wohler Synthesis of Urea

In 19281928, German scientist Fedrick Wohler accidentally synthesized organic urea (NH2CONH2NH_2CONH_2) by heating inorganic ammonium sulphate and potassium cyanate: (NH4)2SO4+2KCNO→2NH4CNO+K2SO4(NH_4)_2SO_4 + 2KCNO \rightarrow 2NH_4CNO + K_2SO_4, followed by molecular rearrangement NH4CNO→NH2CONH2NH_4CNO \rightarrow NH_2CONH_2.

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Catenation in Organic Chemistry

The property of carbon forming covalent bonds with other carbon atoms, leading to over 10 million10\text{ million} organic compounds compared to around 1 million1\text{ million} inorganic compounds.

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Functional Group

A structural feature present only in organic compounds that determines their chemical functions and reactivity.

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Isomerism

A phenomenon present in organic compounds where different compounds share the same molecular formula; it is absent in inorganic compounds.

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Solubility Comparison of Organic and Inorganic Compounds

Organic compounds are generally insoluble in water, whereas inorganic compounds are water-soluble.

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Combustibility Comparison of Organic and Inorganic Compounds

Organic compounds are highly inflammable due to their covalent nature, whereas inorganic compounds are not as highly inflammable.