In the three-step synthesis below, at least one of the steps would fail as shown. For each step. indicate whether each step would succeed or fail by circling the proper answer. If a step would fail briefly describe why and how you would rectify the synthesis. would this step Succeed or Fail (circle one) H₂C Succeed or Fail (circle one) H₂C OH Succeed or Fail (circle one) H₂C OH 1. CH3MgBr (1 Equiv.) 2. H3O* (workup) OH Na₂Cr₂O7 H₂SO4 OH 1. SOCI₂ (converts -OH to -CI) 2. Mg(s), Et₂0 3. 1 4. H₂O* (workup) OH

In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reacti…

A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carboc…

A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond t…

It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthes…

Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.