Chemistry Homework Solutions
#21086
Predict the product of the crossed Cannizzaro reaction
[Question]
[Predict the product of crossed Cannizzaro reaction between formaldehyde and p-anisaldehyde (4-methoxybenzaldehyde).]
In excess formaldehyde, the aromatic aldehyde is reduced to a primary alcohol in high yield.
What is this?
By OTA - Overall OTA Rating
Departed OTA
Purchase Cost Now
$2.19 CAD (was ~$11.97)
Included in Download
- Plain text response
- Attached file(s):
- Hello.doc
Why you can trust BrainMass.com
- Your Information is Secure
- Best Online Academic Help Service
- Students find real academic Success
- Crossed Cannizzaro reaction with Formaldehyde - I am having trouble with this problem. "...crossed Canizzaro reactions can be realized when one of the components is formaldehyde. Predict the products of the reaction below and give a suitable n ...
- mechanism for internal Cannizzaro reaction - Show me a mechanism for this internal Cannizzaro reaction: phthalaldehyde ---> 2-(hydroxymethyl)benzoic acid
- Wittig reaction - geometry of the double bond if aldehyde other than formaldehyde used - If an aldehyde other than formaldehyde were to be used, what would the geometry of the double bond be in the major product and why?
- Wittig reaction and Cannizzaro reaction - Show a step by step mechanism of a Wittig reaction and a Cannizzaro reaction using cinamaldehyde.
- 3 Questions (L4) - 13. Why it is important that any aldehyde used in Witting reaction be free of carboxylic acid impurities? 14. Explain why the C=C stretching mode gives rise to a rather weak IR band in 1-methylcy ...
