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The 161 pages that link to Hydrogen bond, each with the reason it gives.
Double bondCompared with: Despite its name, it is an intermolecular or intramolecular attraction, not a shared-pair covalent bond.
EthanolamineRelated: Its hydroxyl and amino groups promote hydrogen bonding and help it mix with water.
Fatty alcoholRelated: Hydroxyl groups let fatty alcohol molecules hydrogen-bond with one another and with water.
Glycolic acidRelated: Hydrogen bonding helps explain glycolic acid’s strong affinity for water.
AsparagineRelated: Asparagine’s side-chain carbonyl and amide can participate in hydrogen bonding.
LipophilicityRelated: Interactions with water can counteract transfer into nonpolar phases and reduce apparent lipophilicity.
MethylamineRelated: Methylamine molecules can form hydrogen bonds through their N–H bonds and nitrogen lone pairs.
Polar covalent bondRelated: Polar bonds such as O–H create the charged sites that enable hydrogen bonding.
Polyvinyl alcoholBroader topic: Hydrogen bonds between PVA chains help explain its strength and restricted water solubility.
CyclohexanolRelated: Its hydroxyl groups hydrogen-bond, influencing cyclohexanol's boiling point and water solubility.
DimethylamineRelated: Dimethylamine’s N–H bond allows intermolecular hydrogen-bond donation.
Double helixBroader topic: Hydrogen bonds help stabilize complementary base pairs across the helix.
Facial tissueRelated: Hydrogen bonding helps cellulose fibers cohere in the dry sheet.
Hydrogen chalcogenideRelated: Strong hydrogen bonding between water molecules makes water unusual among these compounds.
Hydrogen iodideCompared with: HI does not form the strong hydrogen bonds characteristic of HF.
Hydrogen tellurideCompared with: H₂Te lacks the strong intermolecular hydrogen bonding found in water and hydrogen fluoride.
Methane clathrateRelated: Hydrogen bonds organize water molecules into the clathrate cage framework.
Stearyl alcoholRelated: Hydroxyl groups allow stearyl alcohol molecules to form hydrogen-bond interactions.
Tannic acidRelated: Hydrogen bonding helps tannic acid associate with protein surfaces.
Tritiated waterRelated: Tritiated water retains the hydrogen-bonding interactions that shape liquid water.
1-PropanolRelated: Its hydroxyl groups form hydrogen bonds, helping explain 1-propanol’s boiling point and water solubility.
Arsenous acidRelated: Interactions with water help stabilize dissolved As(OH)₃ despite its instability as an isolated acid.
Cetyl alcoholRelated: Its hydroxyl group can form hydrogen bonds with water and other formulation ingredients.
Crystal engineeringRelated: Directional hydrogen bonds often act as predictable links between molecules in designed crystals.
FormamideRelated: Formamide's N–H bonds and carbonyl oxygen enable strong intermolecular association.
IsobutanolRelated: Its hydroxyl group enables hydrogen bonding, influencing isobutanol’s boiling point and mixing behavior.
PyrogallolRelated: Its three hydroxyl groups allow extensive hydrogen bonding in pyrogallol crystals and solutions.
Trifluoroacetic acidRelated: Hydrogen bonding affects its association and physical behavior in liquid mixtures.
Water memoryBroader topic: Water-memory proposals often attribute persistence to networks of these intermolecular attractions.
1-PentanolRelated: Its hydroxyl groups form hydrogen bonds, affecting boiling point and water solubility.
AcetamideRelated: Acetamide molecules form intermolecular hydrogen bonds through their N–H groups and carbonyl oxygens.
AcetylacetoneRelated: An intramolecular hydrogen bond stabilizes the enol form of acetylacetone.
Argon fluorohydrideCompared with: HArF contains a covalent molecular framework, not merely a hydrogen-bonded HF–argon complex.
Chemical polarityRelated: Polar bonds create the partial charges that enable many hydrogen bonds.
GuanidineRelated: Guanidine and guanidinium form hydrogen bonds with water and biological molecules.
Hair ironRelated: Water and heat disrupt temporary hydrogen bonds in hair, allowing a new shape to set as it cools.
HelicaseRelated: Hydrogen bonds help stabilize paired bases that helicases separate.
HydrophileRelated: Water forms hydrogen bonds with polar groups such as hydroxyls and amines.
HydrophobicityRelated: Water’s hydrogen-bond network helps explain why nonpolar surfaces are unfavorable in water.
ResorcinolRelated: Resorcinol’s hydroxyl groups form hydrogen bonds that influence its physical properties.
ThioureaRelated: Thiourea’s N–H groups shape its crystal packing and interactions with solvents and ions.
1-HexanolRelated: Its hydroxyl groups hydrogen-bond, affecting boiling point and water solubility.
1-OctanolRelated: Its hydroxyl group forms hydrogen bonds, influencing boiling point and interactions with water.
1,4-DioxaneRelated: Water hydrogen-bonds with 1,4-dioxane, supporting its high water solubility.
Ammonium dihydrogen phosphateRelated: Hydrogen bonding helps shape interactions among ions and water in the crystal and its solutions.
Bonding in solidsBroader topic: It helps organize molecular solids such as ice and some organic crystals.
Caesium fluorideRelated: Protic solvents hydrogen-bond to fluoride, reducing its nucleophilicity.
Clathrate compoundCompared with: Clathrate guests are generally retained without the specific directional bonding that defines hydrogen bonds.
Diethylene glycolRelated: Its hydroxyl groups form hydrogen bonds that contribute to its viscosity and water miscibility.
DodecanolRelated: Dodecanol’s hydroxyl groups hydrogen-bond with water and with one another.