What students write about when students write about mechanisms: analysis of features present in students’ written descriptions of an organic reaction mechanism

2020 ◽  
Vol 21 (4) ◽  
pp. 1148-1172
Author(s):  
Field M. Watts ◽  
Jennifer A. Schmidt-McCormack ◽  
Catherine A. Wilhelm ◽  
Ashley Karlin ◽  
Atia Sattar ◽  
...  

Learning to reason through organic reaction mechanisms is challenging for students because of the volume of reactions covered in introductory organic chemistry and the complexity of conceptual knowledge and reasoning skills required to develop meaningful understanding. However, understanding reaction mechanisms is valuable for students because they are useful for predicting and explaining reaction outcomes. To identify the features students find pertinent when explaining reaction mechanisms, we have collected students’ written descriptions of an acid-catalysed amide hydrolysis reaction. Students’ writing was produced during the implementation of Writing-to-Learn assignments in a second semester organic chemistry laboratory course. We analysed students’ written responses using an analytical framework for recognizing students’ mechanistic reasoning, originally developed with attention to the philosophy of science literature. The analysis sought to identify the presence of specific features necessary for mechanistic reasoning belonging to four broad categories: (1) describing an overview of the reaction, (2) detailing the setup conditions required for the mechanism to occur, (3) describing the changes that take place over the course of the mechanism, and (4) identifying the properties of reacting species. This work provides a qualitative description of the variety of ways in which students included these features necessary for mechanistic reasoning in their writing. We additionally analysed instances of co-occurrence for these features in students’ writing to make inferences about students’ mechanistic reasoning, defined here as the use of chemical properties to justify how electrons, atoms, and molecules are reorganized over the course of a reaction. Feature co-occurrences were quantified using the lift metric to measure the degree of their mutual dependence. The quantitative lift results provide empirical support for the hierarchical nature of students’ mechanistic descriptions and indicate the variation in students’ descriptions of mechanistic change in conjunction with appeals to chemistry concepts. This research applies a framework for identifying the features present in students’ written mechanistic descriptions, and illustrates the use of an association metric to make inferences about students’ mechanistic reasoning. The findings reveal the capacity of implementing and analysing writing to make inferences about students’ mechanistic reasoning.

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Sachin Nedungadi ◽  
Corina E. Brown

AbstractThe difficulties students face with organic reaction mechanisms have been the subject of much research in chemical education however, no concept inventory has been reported in this area. The development of a concept inventory would be useful for the large-scale assessment of students’ understanding of concepts pertinent to developing proficiency in reaction mechanisms. The first step in the design of such an inventory is identifying the pertinent concepts. In phase 1 of this study, open-ended interviews were carried out with organic chemistry instructors (N = 11) in order to ascertain their opinions on pertinent concepts for developing proficiency in reaction mechanisms. Phase 2 of the study consisted of a national survey of organic chemistry instructors (N = 183) to explore the general consensus regarding the concepts identified in phase 1. The results yielded 10 concepts identified by experts to be pertinent to reaction mechanisms. The general consensus among organic chemistry instructors is that the topic of reaction mechanisms is important to the study of organic chemistry, but students have difficulty understanding the meaning of the curved-arrow notation. Future work will include the design and development of a concept inventory based on these pertinent concepts.


Author(s):  
Nimesh Mistry ◽  
Stephen Nicholson

The use of laboratory work to improve students’ knowledge of theory is one that is disputed. Student reflections of what they learn during practical work repeatedly show that students rarely think about theory. There is a lack of data that objectively compares students’ knowledge of theory where they complete an associated experiment to when they do not in order to understand if practical work does effect students’ knowledge of scientific concepts. In this work we aimed to address this gap by investigating the effect of students’ knowledge of organic mechanisms where they both perform and associated experiment and where they did not. Our results showed that organic chemistry experiments had no effect on students’ knowledge of organic mechanisms. These results support the view that there is little evidence to support the use of laboratory work to aid understanding of theory.


2014 ◽  
Vol 2014 ◽  
pp. 1-13 ◽  
Author(s):  
Rodrigo Ormazábal-Toledo ◽  
Renato Contreras

Theoretical scales of reactivity and selectivity are important tools to explain and to predict reactivity patterns, including reaction mechanisms. The main achievement of these efforts has been the incorporation of such concepts in advanced texts of organic chemistry. In this way, the modern organic chemistry language has become more quantitative, making the classification of organic reactions an easier task. The reactivity scales are also useful to set up a number of empirical rules that help in rationalizing and in some cases anticipating the possible reaction mechanisms that can be operative in a given organic reaction. In this review, we intend to give a brief but complete account on this matter, introducing the conceptual basis that leads to the definition of reactivity indices amenable to build up quantitative models of reactivity in organic reactions. The emphasis is put on two basic concepts describing electron-rich and electron-deficient systems, namely, nucleophile and electrophiles. We then show that the regional nucleophilicity and electrophilicity become the natural descriptors of electrofugality and nucleofugality, respectively. In this way, we obtain a closed body of concepts that suffices to describe electron releasing and electron accepting molecules together with the description of permanent and leaving groups in addition, nucleophilic substitution and elimination reactions.


2005 ◽  
Vol 83 (9) ◽  
pp. 1400-1414 ◽  
Author(s):  
John Andraos

Scientific genealogy trees of scientists who contributed to the study of organic reaction mechanisms over the last century are presented. The trees show doctoral and post-doctoral connections among scientists as well as connections between scientific ideas. Contributions made by scientists working in laboratories at Canadian universities and at the National Research Council of Canada are noted throughout. These trees, covering more than two centuries, are of interest to senior scientists and young students of science alike in understanding the evolution of scientific ideas and in career development for aspiring scientists. Key patterns revealed by these trees pertaining to ideas and discoveries made, how they were made, connections between them, and who made them are also discussed.Key words: reaction mechanisms, physical organic chemistry, scientific genealogies.


2021 ◽  
Vol 9 (2) ◽  
pp. 6-30
Author(s):  
Nurul Nadiah Rosly ◽  
Shafida Abd Hamid ◽  
Nor Azlina A. Rahman

Students perceive organic chemistry as a challenging subject for them to learn and master, which results in a high failure rate. This study investigates the perception of chemistry students of the Department of Chemistry, Kulliyyah of Science at International Islamic University Malaysia (IIUM), on organic chemistry courses and identify the topics that the students found difficult to grasp, which may affect their grades. The correlation of students’ perception on the difficulty level in studying organic chemistry subjects (I and II) with the grades obtained for both courses, and the correlation of the type of study attitude with the grades achieved for Organic Chemistry I and II, were also investigated. From the data analysis of questionnaires distributed to 160 respondents, stereochemistry (n = 58.8 %), determination of reaction type (n = 59.4 %), construction of the reaction mechanisms (n = 73.2 %), and characterisation of organic reaction (n = 77.5 %), were the topics that the students perceived to be difficult. Perception on the difficulty in studying organic chemistry was positively associated with the achievement of excellent grades for both organic chemistry subjects (I; rs = 0.413**, p<0.01 and II; rs = 0.436**, p<0.01). Quality of study attitude shows no association with the grades obtained for organic chemistry I (rs = 0.330**, p = 1.00) but positively associated with grades of organic chemistry II subject (rs = 0.140, p<0.01). This study could serve as a reference for lecturers to search for ways to design appropriate teaching approaches for better learning experiences.


2019 ◽  
Vol 0 (0) ◽  
Author(s):  
Sachin Nedungadi ◽  
Sue H. Paek ◽  
Corina E. Brown

AbstractUndergraduate organic chemistry has been found to be historically difficult for students and one area where students struggle is organic reaction mechanisms. The difficulties students face with reaction mechanisms has been a source of interest in chemical education research but most studies done have been purely qualitative. An assessment tool that could be used on a large-scale for instructors to gauge the difficulties their students face, would be useful. The aim of this pilot study is to use Rasch analysis to establish the validity and reliability of the concepts important for developing proficiency in organic reaction mechanisms inventory (RMCPI). The test, containing 25 items, was administered to first semester organic chemistry students (N = 44) at a mid-sized university. The data was analyzed using Rasch techniques to explore the dimensionality of the instrument, the difficulty of the items, the item fit, and the reliability. The results indicate that the instrument is unidimensional and most of the items fit well to the dichotomous Rasch model. The test was found to be difficult and this will be explored further by increasing the sample size, administering the test to students from other universities and increasing the number of items on the inventory.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Sachin Nedungadi ◽  
Michael D. Mosher ◽  
Sue Hyeon Paek ◽  
Richard M. Hyslop ◽  
Corina E. Brown

Abstract The fundamental concepts for organic reaction mechanisms inventory (FC-ORMI) is a multiple-choice instrument designed to assess students’ conception of fundamental concepts for understanding organic reaction mechanisms. The concepts were identified from open-ended interviews and a national survey of organic chemistry instructors reported in a previous study. This manuscript describes the development of the inventory items related to these identified concepts and the psychometric analysis of the instrument. In the developmental stage, open-ended questions were administered to first-semester organic chemistry students (N = 138), and open-ended interviews were conducted with students (N = 22) from the same pool to gain insight into their thought processes. The answers revealed alternate conceptions which were used to formulate distractors for the inventory. A pilot version and a beta version of the inventory were administered to 105 and 359 first-semester organic chemistry students, respectively. From these administrations, the 26-item alpha version was developed and administered to first-semester undergraduate organic chemistry students (N = 753). Psychometric analysis was conducted at the item and test level using Classical Test Theory and Rasch analysis. The results indicate that the items on the FC-ORMI function well to reveal students’ alternate conceptions. The instrument meets the acceptable standards of validity and reliability for concept inventories.


Author(s):  
Julia Eckhard ◽  
Marc Rodemer ◽  
Axel Langner ◽  
Sascha Bernholt ◽  
Nicole Graulich

Research in Organic Chemistry education has revealed students’ challenges in mechanistic reasoning. When solving mechanistic tasks, students tend to focus on explicit surface features, apply fragmented conceptual knowledge, rely on rote-memorization and, hence, often struggle to build well-grounded causal explanations. When taking a resource perspective as a lens, students’ difficulties may arise from either an unproductive or a missing activation of cognitive resources. Instructors’ explanations and their guidance in teaching situations could serve as a lynchpin to activate these resources. Compared to students’ challenges in building mechanistic explanations in Organic Chemistry, little is known about instructors’ explanations when solving mechanistic tasks and how they shape their targeted explanations for students in terms of the construction and embedding of cause–effect rationales. This qualitative study aims to contribute to the growing research on mechanistic reasoning by exploring instructors’ explanatory approaches. Therefore, we made use of the framing construct, intended to trigger certain frames with explicit instruction. Ten Organic Chemistry instructors (university professors and lecturers) were asked to solve case comparison tasks while being prompted in two scenarios: an expert frame and a teaching frame. Our analysis shows that there is a shift from instructors’ mechanistic explanations in the expert frame towards more elaborated explanations in the teaching frame. In the teaching frame, contrary to what might be expected, complete cause–effect relationships were not always established and instructors differed in how they shaped their explanations. Additional explanatory elements were identified in both frames and their shift in use is discussed. Comparing approaches between frames sheds light on how instructors communicate mechanistic explanations and allows us to derive implications for teaching Organic Chemistry.


2005 ◽  
Vol 83 (9) ◽  
pp. 1197-1201
Author(s):  
Thomas T Tidwell

Some of the history of the development of physical organic chemistry in Canada from the 1920s is presented, including many of the individuals involved, and their major areas of interest.Key words: history of physical organic chemistry in Canada, organic reaction mechanisms, free radicals, kinetics.


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