Show what reactions occurred with your unknown. Use line-angle structures, show all electrons and lone pairs, and charges. No mechanism is required; just include reactants, conditions, and products.
Acetone was introduced to Br2 in methylene chloride.
Show what reactions occurred with your unknown. Use line-angle structures, show all electrons and lone pairs,...
Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...
Please show the mechanism of reaction for this SN2
reaction. Please include all arrows, lone pairs, charges, and
products. Thanks!
OH CHy
Predict the mechanism for the following reaction (show all steps, include lone pairs, include all byproducts, include all products). CH3 Сгоз H3C H OH Predict the mechanism for the following reaction (show all steps, include lone pairs, include all byproducts, include all products). HNO3 ΝΗ H2SO4 CH3
Write Lewis structures for the molecules represented by the
following line-angle formulas.
a)
Draw the molecule by placing atoms on the grid and
connecting them with bonds. Include all hydrogen atoms. Include all
lone pairs of electrons.
b)
Draw the molecule by placing atoms on the grid and
connecting them with bonds. Include all hydrogen atoms. Include all
lone pairs of electrons.
Determine the products for the acid base reactions
(include lone pairs and formal charges) indicate whether each is a
protonation or deprotonation. then rewrite the first 2 and include
mechanistic arrows to form the products
9. Determine the products for the acid-base reactions show below charges!). Indicate whether each reaction is a protonation or a the products of these acid base reactions have in common? NH HCI OH NaOH OH NaHCO3 OH NaOH 10. Rewrite the first 2 reactions above...
complete the mechanism by drawing proper arrows and show all lone
pairs in the reactants and products
H3C + ONO CH3 сн. н. HC-a. sº H3CCI + O=s=0
Provide a mechanism for formation of the following bromohydrin. Clearly show stereochemistry, all lone pairs, charges and curvy arrows, and show the mechanism in a stepwise manner. DO NOT combine two steps into one! IN YOUR MECHANSIM, ONLY SHOW FORMATION OF ONE ENANTIOMER. a. CH3 Br CH3 Br2 H2o CH-CH, + E CH2CH, OH
Predict the mechanism for the following reaction (show all
steps, include lone pairs, include all byproducts, include all
products).
HNO3 NH H2SO4 OF CH3
Predict the mechanism for the following reaction (show all
steps, include lone pairs, include all byproducts, include all
products).
CH3 Cro Нас н" ОН
Predict the mechanism for the following reaction (show all steps, include lone pairs, include all byproducts, include all products). NH–NH2 CH3 + ON NO2 CH3