Top 10 similar words or synonyms for phch

chph    0.838889

phoch    0.822228

ophch    0.813909

cooet    0.800932

chme    0.797988

ncch    0.794677

occh    0.787811

phnh    0.786964

bnch    0.786709

phcoch    0.785643

Top 30 analogous words or synonyms for phch

Article Example
Kalgachia The Civil Hospital of Barpeta is situated centrally at Kalgachia Town. In spite of that there is also PHCH at Kalgachia Town.
Thiosulfurous acid Four isomers are possible for RSO, at least restricting sulfur to di- and tetravalency: (RO)S=S, ROSSOR, RS(O)SR, and RS(O)SOR. For the first two, the R groups are equivalent, and in the latter two they are nonequivalent. A simple example is diethylthiosulfite, (EtO)S=S. It is also known as diethylthionosulfite. It is a stereochemically rigid on the NMR timescale to about 140 ºC, somewhat similar to diethylsulfoxide. Many derivatives have been prepared from glycols. From meso-hydrobenzoin (PhCH(OH)-CH(OH)Ph), one obtains two isomers; a third isomer results from d,l-PhCH(OH)-CH(OH)Ph.
Benzoin Benzoin ( or ) is an organic compound with the formula PhCH(OH)C(O)Ph. It is a hydroxy ketone attached to two phenyl groups. It appears as off-white crystals, with a light camphor-like odor. Benzoin is synthesized from benzaldehyde in the benzoin condensation. It is chiral and it exists as a pair of enantiomers: ("R")-benzoin and ("S")-benzoin.
Nickel tetracarbonyl Reactions of Ni(CO) with alkyl and aryl halides often result in carbonylated organic products. Vinylic halides, such as PhCH=CHBr, are converted to the unsaturated esters upon treatment with Ni(CO) followed by sodium methoxide. Such reactions also probably proceed via oxidative addition. Allylic halides give the π-allylnickel compounds, such as (allyl)NiCl:
Kinetic isotope effect In this particular "intramolecular KIE" study, a benzylic hydrogen undergoes radical substitution by bromine using "N"-bromosuccinimide as the brominating agent. It was found that PhCH brominates 4.86x faster than PhCD. A large KIE of 5.56 is associated with the reaction of ketones with bromine and sodium hydroxide.