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- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_332_--_Organic_Chemistry_II_(Lund)/1%3A_Fall_term_review_sections/1%3A_Introduction_to_Organic_Structure_and_Bonding_I/1.2%3A_Functional_groups_and_organic_nomenclatureFunctional groups are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms. The structure of capsaicin, the compound discussed in the begi...Functional groups are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms. The structure of capsaicin, the compound discussed in the beginning of this chapter, incorporates several functional groups, labeled in the figure below and explained throughout this section.
- https://chem.libretexts.org/Courses/Clackamas_Community_College/CH_112%3A_Chemistry_for_Health_Sciences/13%3A_Organic_Compounds_of_Oxygen/13.09%3A_EthersTo give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. E...To give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. Ether molecules have no OH group and thus no intermolecular hydrogen bonding. Ethers therefore have quite low boiling points for a given molar mass. Ether molecules have an oxygen atom and can engage in hydrogen bonding with water molecules. An ether molecule has about the same solubility in water as
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/04%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/4.10%3A_Spectroscopy_of_Ethers_and_EpoxidesThe 1 H NMR spectrum of dipropyl ether, Figure \PageIndex{3}, shows three signals with the triplet at 3.37 ppm (B) assigned to the -CH 2 - beside the ether and the other two signals upfield (1.59 ...The 1 H NMR spectrum of dipropyl ether, Figure \PageIndex{3}, shows three signals with the triplet at 3.37 ppm (B) assigned to the -CH 2 - beside the ether and the other two signals upfield (1.59 and 0.93 ppm). Alpha-cleavage at the carbon-carbon bond adjacent to the oxygen atom , leading to the formation of prominent fragment ion m/z = 59, corresponding to the loss of an ethyl radical (m = 29).
- https://chem.libretexts.org/Courses/Victor_Valley_College/CHEM100_Victor_Valley_College/12%3A_Organic_Compounds_of_Oxygen_and_Nitrogen/12.07%3A_EthersTo give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. E...To give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. Ether molecules have no OH group and thus no intermolecular hydrogen bonding. Ethers therefore have quite low boiling points for a given molar mass. Ether molecules have an oxygen atom and can engage in hydrogen bonding with water molecules. An ether molecule has about the same solubility in water as
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Basics_of_General_Organic_and_Biological_Chemistry_(Ball_et_al.)/14%3A_Organic_Compounds_of_Oxygen/14.08%3A_EthersTo give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. E...To give ethers common names, simply name the groups attached to the oxygen atom, followed by the generic name ether. If both groups are the same, the group name should be preceded by the prefix di-. Ether molecules have no OH group and thus no intermolecular hydrogen bonding. Ethers therefore have quite low boiling points for a given molar mass. Ether molecules have an oxygen atom and can engage in hydrogen bonding with water molecules. An ether molecule has about the same solubility in water as
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/18%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/18.02%3A_Names_and_Properties_of_EthersThe bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both ...The bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both having the molecular formula C 2 H 6 O) are completely soluble in water, whereas diethyl ether and 1-butanol (both C 4 H 10 O) are barely soluble in water (8 g/100 mL of water).
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/18%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/18.02%3A_Names_and_Properties_of_EthersThe electronegative oxygen atom gives ethers a slight dipole moment, and the boiling points of ethers are often slightly higher than the boiling points of comparable alkanes. Ethers are relatively sta...The electronegative oxygen atom gives ethers a slight dipole moment, and the boiling points of ethers are often slightly higher than the boiling points of comparable alkanes. Ethers are relatively stable and unreactive in many respects, but some ethers react slowly with the oxygen in air to give peroxides, compounds that contain an O–O bond. Ethers are very useful as solvents in the laboratory, but they must always be used cautiously and should not be stored for long periods of time.
- https://chem.libretexts.org/Courses/Chandler_Gilbert_Community_College/Fundamental_Organic_ala_Mech/04%3A_Functional_Groups/4.08%3A_Names_and_Properties_of_EthersThe electronegative oxygen atom gives ethers a slight dipole moment, and the boiling points of ethers are often slightly higher than the boiling points of comparable alkanes. Ethers are relatively sta...The electronegative oxygen atom gives ethers a slight dipole moment, and the boiling points of ethers are often slightly higher than the boiling points of comparable alkanes. Ethers are relatively stable and unreactive in many respects, but some ethers react slowly with the oxygen in air to give peroxides, compounds that contain an O–O bond. Ethers are very useful as solvents in the laboratory, but they must always be used cautiously and should not be stored for long periods of time.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/EstersEsters are known for their distinctive odors and are commonly used for food aroma and fragrances. The general formula of an ester is RCOOR'.
- https://chem.libretexts.org/Courses/Martin_Luther_College/Organic_Chemistry_-_MLC/03%3A_Alcohols_Ethers_Thiols_Sulfides_and_Amines/3.02%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/3.2.02%3A_Names_and_Properties_of_EthersThe bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both ...The bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both having the molecular formula C 2 H 6 O) are completely soluble in water, whereas diethyl ether and 1-butanol (both C 4 H 10 O) are barely soluble in water (8 g/100 mL of water).
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/18%3A_Ethers_and_Epoxides_Thiols_and_Sulfides/18.01%3A_Names_and_Properties_of_EthersThe bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both ...The bond angle of dimethyl ether is 112 o which is larger than the H-O-H bond angle in water (104.5 o ) due to the steric repulsion of the methyl groups. For example, dimethyl ether and ethanol (both having the molecular formula C 2 H 6 O) are completely soluble in water, whereas diethyl ether and 1-butanol (both C 4 H 10 O) are barely soluble in water (8 g/100 mL of water).
