The compound NaH2PO4 name is
sodium dihydrogen phosphate
Explanation
This name is arrived at by using the IUPAC rules of naming compound
1. the metal (sodium)is named first followed by the ligand ( hydrogen and phosphate)
Ligand are molecules that are attached to the metal center.
2. ligand are named using alphabetical order(for our case h for hydrogen come before p for phosphate hence hydrogen is named first)
3. Prefix di is used since hydrogen are two
hence the name of the compound is Sodium dihydrogen phosphate
Answer:but-1-ene
Explanation:This is an E2 elimination reaction .
Kindly refer the attachment for complete reaction and products.
Sodium tert-butoxide is a bulky base and hence cannot approach the substrate 2-chlorobutane from the more substituted end and hence major product formed here would not be following zaitsev rule of elimination reaction.
Sodium tert-butoxide would approach from the less hindered side that is through the primary centre and hence would lead to the formation of 1-butene .The major product formed in this reaction would be 1-butene .
As the mechanism of the reaction is E-2 so it will be a concerted mechanism and as sodium tert-butoxide will start abstracting the primary hydrogen through the less hindered side simultaneously chlorine will start leaving. As the steric repulsion in this case is less hence the transition state is relatively stabilised and leads to the formation of a kinetic product 1-butene.
Kinetic product are formed when reactions are dependent upon rate and not on thermodynamical stability.
2-butene is more thermodynamically6 stable as compared to 1-butene
The major product formed does not follow the zaitsev rule of forming a more substituted alkene as sodium tert-butoxide cannot approach to abstract the secondary proton due to steric hindrance.
Answer:
mechanical energy to electrical energy to light energy
Potassium is placed where it is based on its properties and it's reactivity. It's also placed there based on it's atomic number.
Answer:
Role is defined below
Explanation:
A small GTP-binding protein, is an important module of the signal transduction pathway used by growth factors to initiate cell growth and differentiation. Cellular activation with growth factors such as epidermal growth factor (EGF) induces Ras to move from an inactive state linked to GDP to an active state linked to GTP. In recent times, a mixture of genetic and biochemical studies has resulted in the elucidation of a signaling pathway that leads from growth factor receptors to Ras. After joining EGF, the EGF receptor tyrosine kinase is activated, which leads to receptor auto phosphorylation in multiple tyrosine residues. Signaling proteins with homology domains Src 2 (SH2) then bind to these phosphorylated residues in tyrosine, initiating multiple signaling cascades. Distinct of these SH2 area proteins, Grb2, exists in the cytoplasm in a preformed complex with a second protein, Son of Sevenless (Sos), which can catalyze the Ras GTP / GDP exchange. After stimulation of the growth factor, the phosphorylated EGF receptor with tyrosine binds to the Grb2 / Sos complex and translocates it to the plasma membrane. It is believed that this translocation brings Sos closer to Ras, which leads to the activation of Ras. In dissimilarity, the insulin receptor does not bind Grb2 directly, but rather induces the tyrosine phosphorylation of two proteins, the substrate-1 insulin receptor and Shc, which bind to the Grb2 / Sos complex. Once Ras is activated, a cascade of protein kinases that are important in a myriad of growth factor responses is stimulated.
